A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960665



Internal ID18595912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14209675..14210936hg38UCSC Ensembl
Innerchr18:14209674..14210935hg19UCSC Ensembl
Innerchr18:14199674..14200935hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381262
hg191262
hg181262
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2657057, nssv2657060, nssv2657062, nssv2657120, nssv2657059, nssv2657058, nssv2657121, nssv2657056, nssv2657064, nssv2657115, nssv2657118, nssv2657114, nssv2657061, nssv2657122, nssv2657119, nssv2657123, nssv2657065, nssv2657063, nssv2657116, nssv2657117
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A5P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960665
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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