A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047325



Internal ID19136544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89149976..89187161hg38UCSC Ensembl
Innerchr13:89802230..89839415hg19UCSC Ensembl
Innerchr13:88600231..88637416hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3837186
hg1937186
hg1837186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1726n100
Supporting Variantsnssv3713265
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)nsv1047325
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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