A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975062



Internal ID18610270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36428199..36435040hg38UCSC Ensembl
Innerchr10:36717127..36723968hg19UCSC Ensembl
Innerchr10:36757133..36763974hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg386842
hg196842
hg186842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761285, nssv2761226, nssv2762066, nssv2764567
SamplesHGDP00665, HGDP00521, HGDP00778, HGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975062
Frequency
Sample Size10
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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