A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022891



Internal ID19112108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7414033..7470668hg38UCSC Ensembl
Innerchr5:7414146..7470781hg19UCSC Ensembl
Innerchr5:7467146..7523781hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3856636
hg1956636
hg1856636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5562n100
Supporting Variantsnssv3746288, nssv3639640, nssv3639639, nssv3639638
Samples
Known GenesADCY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022891
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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