A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3974371



Internal ID19239210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:194581801..194581878hg38UCSC Ensembl
Outerchr3:194302530..194302607hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114469
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3974371
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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