A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970819



Internal ID18606041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36811267..36823472hg38UCSC Ensembl
Innerchr7:36850872..36863077hg19UCSC Ensembl
Innerchr7:36817397..36829602hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3812206
hg1912206
hg1812206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2443709, nssv2443706, nssv2443705, nssv2443713, nssv2443711, nssv2443712, nssv2443707, nssv2443710, nssv2443714, nssv2443708
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)nsv970819
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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