A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692392



Internal ID18643987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4490134..4604192hg38UCSC Ensembl
Innerchr9:4490134..4604192hg19UCSC Ensembl
Innerchr9:4480134..4594192hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38114059
hg19114059
hg18114059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022493
Supporting Variants
Samples
Known GenesSLC1A1, SPATA6L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692392
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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