A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661263



Internal ID18959544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50190154..50219315hg38UCSC Ensembl
Innerchr7:50229750..50258911hg19UCSC Ensembl
Innerchr7:50200296..50229457hg18UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3829162
hg1929162
hg1829162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020285
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3661263
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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