A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036674



Internal ID19125893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39267345..39433980hg38UCSC Ensembl
Innerchr13:39841482..40008117hg19UCSC Ensembl
Innerchr13:38739482..38906117hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38166636
hg19166636
hg18166636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523387
Samples
Known GenesLHFP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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