A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025542



Internal ID19114760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:162695..379494hg38UCSC Ensembl
Innerchr9:162695..379494hg19UCSC Ensembl
Innerchr9:152695..369494hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38216800
hg19216800
hg18216800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7350n100
Supporting Variantsnssv3690977
Samples
Known GenesC9orf66, CBWD1, DOCK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025542
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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