A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970855



Internal ID18606077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64499036..64563353hg38UCSC Ensembl
Innerchr7:63959414..64023731hg19UCSC Ensembl
Innerchr7:63596849..63661166hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3864318
hg1964318
hg1864318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2456423, nssv2456429, nssv2456426, nssv2456431, nssv2456432, nssv2456430, nssv2456428, nssv2456424, nssv2456427, nssv2456425
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF680
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970855
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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