A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982402



Internal ID18617597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40263761..40269664hg38UCSC Ensembl
Innerchr9:42408779..42414682hg19UCSC Ensembl
Innerchr9:42398775..42404678hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385904
hg195904
hg185904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2729475, nssv2729413, nssv2729473, nssv2729472, nssv2729412, nssv2729414, nssv2729420, nssv2729415, nssv2729470, nssv2729477, nssv2729478, nssv2729476, nssv2729474, nssv2729411, nssv2729471, nssv2729416, nssv2729469, nssv2729417, nssv2729419, nssv2729418
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)nsv982402
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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