A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056184



Internal ID19145403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3093486..3195718hg38UCSC Ensembl
Innerchr17:2996780..3099012hg19UCSC Ensembl
Innerchr17:2943530..3045762hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38102233
hg19102233
hg18102233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560088
Samples
Known GenesOR1G1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056184
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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