A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982401



Internal ID18617596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40261205..40262739hg38UCSC Ensembl
Innerchr9:42406223..42407757hg19UCSC Ensembl
Innerchr9:42396219..42397753hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg381535
hg191535
hg181535
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2727932, nssv2727931, nssv2727930, nssv2727929, nssv2727933, nssv2727938, nssv2727934, nssv2727935, nssv2727936, nssv2727937
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982401
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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