A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970529



Internal ID18259065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73148819..73156302hg38UCSC Ensembl
Innerchr7:72562914..72570388hg19UCSC Ensembl
Innerchr7:72200850..72208324hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387484
hg197475
hg187475
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2463892, nssv2463898, nssv2463893, nssv2463895, nssv2463894, nssv2463896, nssv2463897, nssv2463889, nssv2463890, nssv2463891
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesGTF2IP1, LOC100093631
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970529
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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