A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966801



Internal ID18602031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57049250..57144047hg38UCSC Ensembl
Innerchr7:57116957..57211754hg19UCSC Ensembl
Innerchr7:57120899..57215696hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3894798
hg1994798
hg1894798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2452584, nssv2452581, nssv2452583, nssv2452587, nssv2452586, nssv2452579, nssv2452585, nssv2452588, nssv2452582, nssv2452580
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF479
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966801
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer