A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031655



Internal ID18774189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28884645..29183431hg38UCSC Ensembl
Innerchr9:28884643..29183429hg19UCSC Ensembl
Innerchr9:28874643..29173429hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38298787
hg19298787
hg18298787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7498n100
Supporting Variantsnssv3755901
Samples
Known GenesLINGO2, MIR873
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031655
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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