A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15231506



Internal ID6379520
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636298
Supporting Variants
SamplesNA20320
Known GenesCATSPER2P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15231506
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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