A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970856



Internal ID18606078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64665878..64695443hg38UCSC Ensembl
Innerchr7:64126256..64155821hg19UCSC Ensembl
Innerchr7:63763691..63793256hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3829566
hg1929566
hg1829566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2456031, nssv2456025, nssv2456029, nssv2456033, nssv2456030, nssv2456032, nssv2456024, nssv2456026, nssv2456028, nssv2456027
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR6839, ZNF107
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970856
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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