A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664235



Internal ID18962516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136252401..136298936hg38UCSC Ensembl
Innerchr7:135937149..135983684hg19UCSC Ensembl
Innerchr7:135587689..135634224hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3846536
hg1946536
hg1846536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016275
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)nssv3664235
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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