A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2766437



Internal ID17768516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176400442..176407923hg38UCSC Ensembl
Innerchr2:177265170..177272651hg19UCSC Ensembl
Innerchr2:176973416..176980897hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg387482
hg197482
hg187482
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv979366
Supporting Variants
SamplesHGDP00542
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2766437
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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