A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051463



Internal ID19140682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89149948..89187161hg38UCSC Ensembl
Innerchr13:89802202..89839415hg19UCSC Ensembl
Innerchr13:88600203..88637416hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3837214
hg1937214
hg1837214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1726n100
Supporting Variantsnssv3525462, nssv3525461, nssv3713264, nssv3525463, nssv3525459, nssv3525466, nssv3525467, nssv3525465, nssv3525464, nssv3525460
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)nsv1051463
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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