A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969510



Internal ID18899199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:194347571..194348271hg38UCSC Ensembl
Outerchr3:194068300..194069000hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122074
Supporting Variants
SamplesKWS2
Known GenesCPN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969510
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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