A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030725



Internal ID19119944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1723364..1760672hg38UCSC Ensembl
Innerchr9:1723364..1760672hg19UCSC Ensembl
Innerchr9:1713364..1750672hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3837309
hg1937309
hg1837309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7375n100
Supporting Variantsnssv3692355
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030725
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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