A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027911



Internal ID19117129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39441317..39504158hg38UCSC Ensembl
Innerchr8:39298836..39361677hg19UCSC Ensembl
Innerchr8:39417993..39480834hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3862842
hg1962842
hg1862842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7178n100
Supporting Variantsnssv3685980, nssv3685979
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)nsv1027911
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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