A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055315



Internal ID18797846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54031269..54041522hg38UCSC Ensembl
Innerchr20:52647808..52658061hg19UCSC Ensembl
Innerchr20:52081215..52091468hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810254
hg1910254
hg1810254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4328n100
Supporting Variantsnssv3586100
Samples
Known GenesBCAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055315
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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