A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755935



Internal ID18707530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38451767..38640564hg38UCSC Ensembl
Innerchr9:38451764..38640561hg19UCSC Ensembl
Innerchr9:38441764..38630561hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38188798
hg19188798
hg18188798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028978
Supporting Variants
Samples
Known GenesANKRD18A, FAM201A, FAM95C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755935
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