A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975795



Internal ID18611002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30827856..30832820hg38UCSC Ensembl
Innerchr10:31116785..31121749hg19UCSC Ensembl
Innerchr10:31156791..31161755hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg384965
hg194965
hg184965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762180
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975795
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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