A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020610



Internal ID19109829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176425171..176683001hg38UCSC Ensembl
Innerchr4:177346322..177604152hg19UCSC Ensembl
Innerchr4:177583316..177841146hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38257831
hg19257831
hg18257831
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635460
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)nsv1020610
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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