A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256421



Internal ID5599788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56225444..56240092hg38UCSC Ensembl
Innerchr15:56225944..56239592hg38UCSC Ensembl
Outerchr15:56224444..56241092hg38UCSC Ensembl
chr15:56517642..56532290hg19UCSC Ensembl
Innerchr15:56518142..56531790hg19UCSC Ensembl
Outerchr15:56516642..56533290hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3814649
hg1914649
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636578
Supporting Variants
SamplesNA19035
Known GenesRFX7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15256421
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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