A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015519



Internal ID19104736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39389580..39466943hg38UCSC Ensembl
Innerchr8:39247099..39324462hg19UCSC Ensembl
Innerchr8:39366256..39443619hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3877364
hg1977364
hg1877364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7176n100
Supporting Variantsnssv3756685
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015519
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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