A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964394



Internal ID18252946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36044554..36050516hg38UCSC Ensembl
Innerchr20:34632476..34638438hg19UCSC Ensembl
Innerchr20:34095890..34101852hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg385963
hg195963
hg185963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2235084, nssv2235085, nssv2235089, nssv2235080, nssv2235088, nssv2235081, nssv2235086, nssv2235083, nssv2235087, nssv2235082
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLINC00657
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964394
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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