A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970813



Internal ID18606035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35054143..35077800hg38UCSC Ensembl
Innerchr7:35093755..35117412hg19UCSC Ensembl
Innerchr7:35060280..35083937hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3823658
hg1923658
hg1823658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2442478, nssv2442485, nssv2442482, nssv2442477, nssv2442476, nssv2442483, nssv2442480, nssv2442484, nssv2442481, nssv2442479
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970813
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