A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966745



Internal ID18255289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2671601..2682592hg38UCSC Ensembl
Innerchr7:2711235..2722226hg19UCSC Ensembl
Innerchr7:2677761..2688752hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3810992
hg1910992
hg1810992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2434241, nssv2434240, nssv2434232, nssv2434236, nssv2434233, nssv2434238, nssv2434237, nssv2434239, nssv2434235, nssv2434234
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesAMZ1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966745
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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