A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970932



Internal ID18606154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:113116180..113117907hg38UCSC Ensembl
Innerchr7:112756235..112757962hg19UCSC Ensembl
Innerchr7:112543471..112545198hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg381728
hg191728
hg181728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2475644, nssv2475649, nssv2475645, nssv2475651, nssv2475642, nssv2475650, nssv2475646, nssv2475647, nssv2475648, nssv2475643
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00998
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970932
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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