A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038179



Internal ID19127398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86547718..86739486hg38UCSC Ensembl
Innerchr13:87199973..87391741hg19UCSC Ensembl
Innerchr13:85997974..86189742hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38191769
hg19191769
hg18191769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525435
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038179
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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