A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970442



Internal ID18605664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6329643..6330643hg38UCSC Ensembl
Innerchr7:6369274..6370274hg19UCSC Ensembl
Innerchr7:6335799..6336799hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2434573, nssv2434572, nssv2434576, nssv2434578, nssv2434579, nssv2434577, nssv2434570, nssv2434574, nssv2434571, nssv2434575
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM220A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970442
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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