A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017204



Internal ID18759739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6731786..6775107hg38UCSC Ensembl
Innerchr9:6731786..6775107hg19UCSC Ensembl
Innerchr9:6721786..6765107hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3843322
hg1943322
hg1843322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7391n100
Supporting Variantsnssv3689095
Samples
Known GenesKDM4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017204
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer