A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761185



Internal ID17733093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17827729..17831935hg38UCSC Ensembl
Innerchr10:17869728..17873934hg19UCSC Ensembl
Innerchr10:17909734..17913940hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg384207
hg194207
hg184207
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971903
Supporting Variants
SamplesHGDP00456
Known GenesMRC1
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761185
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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