A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3587558



Internal ID18539153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54035070..54049092hg38UCSC Ensembl
Innerchr20:52651609..52665631hg19UCSC Ensembl
Innerchr20:52085016..52099038hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3814023
hg1914023
hg1814023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067083
Supporting Variants
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)nssv3587558
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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