A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029165



Internal ID19118384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39426730..39531593hg38UCSC Ensembl
Innerchr8:39284249..39389112hg19UCSC Ensembl
Innerchr8:39403406..39508269hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38104864
hg19104864
hg18104864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7181n100
Supporting Variantsnssv3757163
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)nsv1029165
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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