A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030076



Internal ID19119295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101853951..101884230hg38UCSC Ensembl
Innerchr8:102866179..102896458hg19UCSC Ensembl
Innerchr8:102935355..102965634hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3830280
hg1930280
hg1830280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691253, nssv3691252, nssv3691251
Samples
Known GenesNCALD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030076
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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