A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661258



Internal ID18959539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:48879443..49092264hg38UCSC Ensembl
Innerchr7:48919039..49131860hg19UCSC Ensembl
Innerchr7:48889585..49102406hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38212822
hg19212822
hg18212822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021166
Supporting Variants
Samples
Known GenesCDC14C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661258
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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