A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636263



Internal ID6676372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42288763..42328316hg38UCSC Ensembl
Innerchr15:42288763..42328316hg38UCSC Ensembl
Outerchr15:42288263..42328816hg38UCSC Ensembl
chr15:42580961..42620514hg19UCSC Ensembl
Innerchr15:42580961..42620514hg19UCSC Ensembl
Outerchr15:42580461..42621014hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3839554
hg1939554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15230843
SamplesNA19922
Known GenesGANC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636263
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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