A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976651



Internal ID19243342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:161651810..161657210hg38UCSC Ensembl
Outerchr1:161621600..161627000hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124597
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976651
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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