A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966638



Internal ID19242529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:96865944..97068444hg38UCSC Ensembl
Outerchr1:97331500..97534000hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38202501
hg19202501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112538
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966638
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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