A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664242



Internal ID18615837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138478424..138894773hg38UCSC Ensembl
Innerchr7:138163169..138579519hg19UCSC Ensembl
Innerchr7:137813709..138230059hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38416350
hg19416351
hg18416351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030956
Supporting Variants
Samples
Known GenesATP6V0A4, KIAA1549, SVOPL, TMEM213, TRIM24
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3664242
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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