A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15325952



Internal ID3199536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95221726..95227357hg38UCSC Ensembl
Innerchr15:95221776..95227307hg38UCSC Ensembl
Outerchr15:95221674..95227409hg38UCSC Ensembl
chr15:95764955..95770586hg19UCSC Ensembl
Innerchr15:95765005..95770536hg19UCSC Ensembl
Outerchr15:95764903..95770638hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385632
hg195632
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637327
Supporting Variants
SamplesHG02810
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15325952
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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