A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031663



Internal ID19120885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:109165203..109290856hg38UCSC Ensembl
Innerchr8:110177432..110303085hg19UCSC Ensembl
Innerchr8:110246608..110372261hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38125654
hg19125654
hg18125654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7281n100
Supporting Variantsnssv3757338
Samples
Known GenesNUDCD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031663
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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