A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032605



Internal ID19121827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39441317..39526593hg38UCSC Ensembl
Innerchr8:39298836..39384112hg19UCSC Ensembl
Innerchr8:39417993..39503269hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3885277
hg1985277
hg1885277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7181n100
Supporting Variantsnssv3686005, nssv3686015, nssv3686007, nssv3686009, nssv3686010, nssv3686004, nssv3686014, nssv3686008, nssv3686013, nssv3686012, nssv3686003, nssv3686002, nssv3686006, nssv3686011
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)nsv1032605
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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