A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655074



Internal ID18606669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6317073..6370187hg38UCSC Ensembl
Innerchr7:6356704..6409818hg19UCSC Ensembl
Innerchr7:6323229..6376343hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3853115
hg1953115
hg1853115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025381
Supporting Variants
Samples
Known GenesFAM220A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655074
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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