A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991795



Internal ID18891089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:155025787..155025852hg38UCSC Ensembl
Outerchr3:154743576..154743641hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139171
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991795
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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