A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982613



Internal ID19214772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136302225..136307375hg38UCSC Ensembl
Outerchr3:136021067..136026217hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385151
hg195151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145460
Supporting Variants
SamplesKWS1
Known GenesPCCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982613
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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