A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963136



Internal ID19244038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64340887..64341306hg38UCSC Ensembl
Outerchr15:64633086..64633505hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38420
hg19420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120703
Supporting Variants
SamplesKWS2
Known GenesCSNK1G1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963136
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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