A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045137



Internal ID19134356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87547782..87618394hg38UCSC Ensembl
Innerchr13:88200037..88270649hg19UCSC Ensembl
Innerchr13:86998038..87068650hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3870613
hg1970613
hg1870613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1725n100
Supporting Variantsnssv3525448
Samples
Known GenesMIR4500HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045137
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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