A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983625



Internal ID18618818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18831586..18848373hg38UCSC Ensembl
Innerchr13:19405726..19422513hg19UCSC Ensembl
Innerchr13:18303726..18320513hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3816788
hg1916788
hg1816788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2620555, nssv2620554, nssv2620552, nssv2620548, nssv2620547, nssv2620550, nssv2620549, nssv2620546, nssv2620551, nssv2620553
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A9P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983625
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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