A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964024



Internal ID18599262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:483015..491036hg38UCSC Ensembl
Innerchr4:476804..484825hg19UCSC Ensembl
Innerchr4:466804..474825hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg388022
hg198022
hg188022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2309600, nssv2309596, nssv2309601, nssv2309605, nssv2309602, nssv2309603, nssv2309597, nssv2309604, nssv2309598, nssv2309599
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF721
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964024
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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