A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034650



Internal ID19123871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39426730..39526593hg38UCSC Ensembl
Innerchr8:39284249..39384112hg19UCSC Ensembl
Innerchr8:39403406..39503269hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3899864
hg1999864
hg1899864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7181n100
Supporting Variantsnssv3685955, nssv3685952, nssv3685954, nssv3685953
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034650
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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