A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636298



Internal ID7023094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43742402..43742997hg38UCSC Ensembl
Innerchr15:43742452..43742947hg38UCSC Ensembl
Outerchr15:43742352..43743047hg38UCSC Ensembl
chr15:44034600..44035195hg19UCSC Ensembl
Innerchr15:44034650..44035145hg19UCSC Ensembl
Outerchr15:44034550..44035245hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231505, essv15231503, essv15231504, essv15231502, essv15231506
SamplesNA20320, HG00458, HG02054, HG02470, HG02760
Known GenesCATSPER2P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636298
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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