A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045652



Internal ID19134871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55562607..55839025hg38UCSC Ensembl
Innerchr13:56136742..56413159hg19UCSC Ensembl
Innerchr13:55034743..55311160hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38276419
hg19276418
hg18276418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3714990
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)nsv1045652
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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