A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973347



Internal ID18608562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64410989..64415365hg38UCSC Ensembl
Innerchr9:69423407..69427783hg19UCSC Ensembl
Innerchr9:68713227..68717603hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg384377
hg194377
hg184377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2743035, nssv2743031, nssv2742965, nssv2743028, nssv2742964, nssv2742959, nssv2743032, nssv2743029, nssv2742962, nssv2743030, nssv2742963, nssv2742956, nssv2743034, nssv2742957, nssv2742961, nssv2743033, nssv2742958, nssv2743027, nssv2742960, nssv2743026
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973347
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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