A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020528



Internal ID19109747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:112943501..112987629hg38UCSC Ensembl
Innerchr8:113955730..113999858hg19UCSC Ensembl
Innerchr8:114024906..114069034hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3844129
hg1944129
hg1844129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7285n100
Supporting Variantsnssv3691305, nssv3691306, nssv3691304
Samples
Known GenesCSMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020528
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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