A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016345



Internal ID19105564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32169581..32382465hg38UCSC Ensembl
Innerchr7:32209193..32422077hg19UCSC Ensembl
Innerchr7:32175718..32388602hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38212885
hg19212885
hg18212885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6318n100
Supporting Variantsnssv3643363
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)nsv1016345
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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