A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020230



Internal ID19109449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25609724..25743451hg38UCSC Ensembl
Innerchr7:25649344..25783071hg19UCSC Ensembl
Innerchr7:25615869..25749596hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38133728
hg19133728
hg18133728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643310
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)nsv1020230
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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