A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968356



Internal ID18603584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181429192..181433018hg38UCSC Ensembl
Innerchr5:180856193..180860019hg19UCSC Ensembl
Innerchr5:180788799..180792625hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg383827
hg193827
hg183827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2705037, nssv2705033, nssv2705035, nssv2705034, nssv2705029, nssv2705038, nssv2705030, nssv2705036, nssv2705032, nssv2705031
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968356
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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