A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2764370



Internal ID17859181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:68087758..68090922hg38UCSC Ensembl
Innerchr2:68314890..68318054hg19UCSC Ensembl
Innerchr2:68168394..68171558hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383165
hg193165
hg183165
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv961754
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2764370
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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