A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017704



Internal ID19106921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28593232..28761733hg38UCSC Ensembl
Innerchr9:28593230..28761731hg19UCSC Ensembl
Innerchr9:28583230..28751731hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38168502
hg19168502
hg18168502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7491n100
Supporting Variantsnssv3692060, nssv3688710
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017704
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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