A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965715



Internal ID18600945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35023464..35024212hg38UCSC Ensembl
Innerchr6:34991241..34991989hg19UCSC Ensembl
Innerchr6:35099219..35099967hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38749
hg19749
hg18749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2405090, nssv2405091, nssv2405095, nssv2405088, nssv2405086, nssv2405089, nssv2405093, nssv2405092, nssv2405094, nssv2405087
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKS1A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965715
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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