A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970584



Internal ID18605806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138623100..138624447hg38UCSC Ensembl
Innerchr7:138307845..138309192hg19UCSC Ensembl
Innerchr7:137958385..137959732hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381348
hg191348
hg181348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2479739, nssv2479740, nssv2479736, nssv2479738, nssv2479735, nssv2479741, nssv2479742, nssv2479737, nssv2479744, nssv2479743
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSVOPL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970584
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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