A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970910



Internal ID18606132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99635038..99636645hg38UCSC Ensembl
Innerchr7:99232661..99234268hg19UCSC Ensembl
Innerchr7:99070597..99072204hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381608
hg191608
hg181608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2470724, nssv2470717, nssv2470722, nssv2470723, nssv2470720, nssv2470718, nssv2470721, nssv2470719, nssv2470715, nssv2470716
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)nsv970910
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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