A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022870



Internal ID18765404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4416046..4611901hg38UCSC Ensembl
Innerchr9:4416046..4611901hg19UCSC Ensembl
Innerchr9:4406046..4601901hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38195856
hg19195856
hg18195856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692390
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)nsv1022870
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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