A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024324



Internal ID18766857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6308178..6408875hg38UCSC Ensembl
Innerchr9:6308178..6408875hg19UCSC Ensembl
Innerchr9:6298178..6398875hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38100698
hg19100698
hg18100698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7387n100
Supporting Variantsnssv3692429
Samples
Known GenesTPD52L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024324
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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