A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027061



Internal ID19116280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39429319..39529434hg38UCSC Ensembl
Innerchr8:39286838..39386953hg19UCSC Ensembl
Innerchr8:39405995..39506110hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38100116
hg19100116
hg18100116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7180n100
Supporting Variantsnssv3685965, nssv3685966
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)nsv1027061
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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