A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031096



Internal ID19120317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108694099..108955957hg38UCSC Ensembl
Innerchr7:108334543..108596014hg19UCSC Ensembl
Innerchr7:108121779..108383250hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38261859
hg19261472
hg18261472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656226, nssv3656227, nssv3656225
Samples
Known GenesC7orf66
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031096
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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