A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1082663



Internal ID15935849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32169747..32360221hg38UCSC Ensembl
Innerchr7:32209359..32399833hg19UCSC Ensembl
Innerchr7:32175884..32366358hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38190475
hg19190475
hg18190475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606592
Supporting Variants
Samples
Known GenesPDE1C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1082663
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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