A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981766



Internal ID19219992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:71582849..71585349hg38UCSC Ensembl
Outerchr3:71632000..71634500hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118976
Supporting Variants
SamplesKWS1
Known GenesFOXP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981766
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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