A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035960



Internal ID19125179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18592436..18795440hg38UCSC Ensembl
Innerchr13:19166576..19369580hg19UCSC Ensembl
Innerchr13:18064576..18267580hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38203005
hg19203005
hg18203005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1603n100
Supporting Variantsnssv3527553
Samples
Known GenesLINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035960
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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