A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970829



Internal ID18606051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:48924878..48929071hg38UCSC Ensembl
Innerchr7:48964474..48968667hg19UCSC Ensembl
Innerchr7:48935020..48939213hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg384194
hg194194
hg184194
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2448255, nssv2448256, nssv2448250, nssv2448249, nssv2448254, nssv2448257, nssv2448248, nssv2448251, nssv2448253, nssv2448252
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCDC14C
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970829
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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