A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984918



Internal ID19212498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:72446949..72447349hg38UCSC Ensembl
Outerchr3:72496100..72496500hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126652
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984918
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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