A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961729



Internal ID19223967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:36354808..36375408hg38UCSC Ensembl
Outerchr3:36396300..36416900hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3820601
hg1920601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129056
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961729
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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