A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973696



Internal ID18608911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42871044..42873510hg38UCSC Ensembl
Innerchr9:67945247..67947712hg19UCSC Ensembl
Innerchr9:67535067..67537532hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382467
hg192466
hg182466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2739200, nssv2739205, nssv2739196, nssv2739198, nssv2739199, nssv2739204, nssv2739201, nssv2739203, nssv2739197, nssv2739202
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973696
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer