A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956568



Internal ID19206187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:16774319..16774482hg38UCSC Ensembl
Outerchr3:16815826..16815989hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116972
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956568
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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