A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963651



Internal ID19234876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82882858..82888917hg38UCSC Ensembl
Outerchr15:83551610..83557669hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386060
hg196060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111515
Supporting Variants
SamplesKWS2
Known GenesHOMER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963651
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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