A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025317



Internal ID19114535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39426673..39511377hg38UCSC Ensembl
Innerchr8:39284192..39368896hg19UCSC Ensembl
Innerchr8:39403349..39488053hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3884705
hg1984705
hg1884705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7178n100
Supporting Variantsnssv3757156
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)nsv1025317
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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