A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979825



Internal ID18615026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44566255..44568129hg38UCSC Ensembl
Innerchr3:44607747..44609621hg19UCSC Ensembl
Innerchr3:44582751..44584625hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381875
hg191875
hg181875
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2278523, nssv2278515, nssv2278514, nssv2278519, nssv2278517, nssv2278520, nssv2278518, nssv2278522, nssv2278516, nssv2278521
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZKSCAN7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979825
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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