A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964837



Internal ID19238017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25686249..25687233hg38UCSC Ensembl
Outerchr15:25931396..25932380hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121145
Supporting Variants
SamplesKWS2
Known GenesATP10A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964837
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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