A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024971



Internal ID19114189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176923673..176968410hg38UCSC Ensembl
Innerchr5:176350674..176395411hg19UCSC Ensembl
Innerchr5:176283280..176328017hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3844738
hg1944738
hg1844738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649284
Samples
Known GenesUIMC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024971
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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