A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713262



Internal ID19011543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87547782..87624536hg38UCSC Ensembl
Innerchr13:88200037..88276791hg19UCSC Ensembl
Innerchr13:86998038..87074792hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3876755
hg1976755
hg1876755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046433
Supporting Variants
Samples
Known GenesMIR4500, MIR4500HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713262
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer