A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637429



Internal ID7024221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99510839..99517472hg38UCSC Ensembl
Innerchr15:99510849..99517462hg38UCSC Ensembl
Outerchr15:99510829..99517482hg38UCSC Ensembl
chr15:100051044..100057677hg19UCSC Ensembl
Innerchr15:100051054..100057667hg19UCSC Ensembl
Outerchr15:100051034..100057687hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg386634
hg196634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15345180, essv15345178, essv15345188, essv15345177, essv15345179, essv15345183, essv15345186, essv15345189, essv15345184, essv15345182, essv15345187, essv15345181, essv15345185, essv15345176
SamplesNA18486, HG03133, NA20317, HG02489, HG02703, HG03225, NA20318, HG02976, HG03382, NA19309, NA19256, HG02839, HG02317, HG03063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637429
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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