A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966781



Internal ID18602011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38655128..38656873hg38UCSC Ensembl
Innerchr7:38694728..38696473hg19UCSC Ensembl
Innerchr7:38661253..38662998hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381746
hg191746
hg181746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2443882, nssv2443877, nssv2443874, nssv2443878, nssv2443879, nssv2443880, nssv2443876, nssv2443881, nssv2443883, nssv2443875
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)nsv966781
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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