A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15195241



Internal ID4466801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26737297..26738664hg38UCSC Ensembl
Innerchr15:26737313..26738649hg38UCSC Ensembl
Outerchr15:26737282..26738680hg38UCSC Ensembl
chr15:26982444..26983811hg19UCSC Ensembl
Innerchr15:26982460..26983796hg19UCSC Ensembl
Outerchr15:26982429..26983827hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg381368
hg191368
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635961
Supporting Variants
SamplesHG03971
Known GenesGABRB3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15195241
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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