A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637194



Internal ID6677301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89416268..89418428hg38UCSC Ensembl
Innerchr15:89416268..89418428hg38UCSC Ensembl
Outerchr15:89416000..89418844hg38UCSC Ensembl
chr15:89959499..89961659hg19UCSC Ensembl
Innerchr15:89959499..89961659hg19UCSC Ensembl
Outerchr15:89959231..89962075hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382161
hg192161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317154, essv15317156, essv15317143, essv15317135, essv15317133, essv15317137, essv15317153, essv15317157, essv15317140, essv15317150, essv15317139, essv15317132, essv15317145, essv15317148, essv15317146, essv15317158, essv15317151, essv15317131, essv15317152, essv15317138, essv15317136, essv15317155, essv15317141, essv15317142, essv15317147, essv15317144, essv15317149, essv15317134
SamplesHG01850, NA19020, HG01806, HG02058, HG02382, HG02356, NA19443, HG02023, HG02374, HG01840, HG02136, HG01841, HG00598, HG02522, HG02165, HG00692, HG02081, HG02184, NA18531, HG01596, NA18646, NA18628, HG02137, HG02128, HG02367, HG01804, HG01872, HG00978
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637194
Frequency
Sample Size2504
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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