A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6353938



Internal ID9331341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24581704..24829462hg38UCSC Ensembl
Outerchr15:24581670..24829497hg38UCSC Ensembl
Innerchr15:24826851..25074609hg19UCSC Ensembl
Outerchr15:24826817..25074644hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38247828
hg19247828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674507
Supporting Variants
SamplesNA20755
Known GenesNPAP1, PWRN1, SNRPN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6353938
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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