A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033812



Internal ID19123033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32169747..32386826hg38UCSC Ensembl
Innerchr7:32209359..32426438hg19UCSC Ensembl
Innerchr7:32175884..32392963hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38217080
hg19217080
hg18217080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6318n100
Supporting Variantsnssv3643366
Samples
Known GenesPDE1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033812
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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