A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036395



Internal ID19125614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48861276..48897062hg38UCSC Ensembl
Innerchr13:49435412..49471198hg19UCSC Ensembl
Innerchr13:48333413..48369199hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3835787
hg1935787
hg1835787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523452, nssv3523451
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)nsv1036395
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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