A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023966



Internal ID18766499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:179188..231133hg38UCSC Ensembl
Innerchr7:179188..231133hg19UCSC Ensembl
Innerchr7:274271..326216hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3851946
hg1951946
hg1851946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654219
Samples
Known GenesFAM20C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023966
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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