A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635961



Internal ID7022758
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15195241
SamplesHG03971
Known GenesGABRB3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635961
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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