A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516024



Internal ID15096631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129747540..129805111hg38UCSC Ensembl
Innerchr7:129387380..129444951hg19UCSC Ensembl
Innerchr7:129174616..129232187hg18UCSC Ensembl
Innerchr7:128981331..129038902hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3857572
hg1957572
hg1857572
hg1757572
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674207, nssv679909, nssv702625, nssv698875, nssv689985, nssv675711, nssv683292, nssv660137, nssv671727, nssv665786, nssv696208, nssv676436
Samples
Known GenesMIR182, MIR183, MIR96, NRF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516024
Frequency
Sample Size2026
Observed Gain1
Observed Loss11
Observed Complex0
Frequencyn/a


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