A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055040



Internal ID19144259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102502623..102593296hg38UCSC Ensembl
Innerchr9:105264905..105355578hg19UCSC Ensembl
Innerchr9:104304726..104395399hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3890674
hg1990674
hg1890674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697588
Samples
Known GenesLINC00587
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055040
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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