A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961730



Internal ID19213036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:42796908..42800508hg38UCSC Ensembl
Outerchr3:42838400..42842000hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383601
hg193601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129057
Supporting Variants
SamplesKWS1
Known GenesHIGD1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961730
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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