A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963831



Internal ID19220305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:67485721..67489521hg38UCSC Ensembl
Outerchr15:67778059..67781859hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383801
hg193801
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129568
Supporting Variants
SamplesKWS1
Known GenesIQCH, IQCH-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963831
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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