A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065562



Internal ID18808093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38271961..38345891hg38UCSC Ensembl
Innerchr20:36900363..36974294hg19UCSC Ensembl
Innerchr20:36333777..36407708hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3873931
hg1973932
hg1873932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4309n100
Supporting Variantsnssv3584772
Samples
Known GenesBPI, LOC149684
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065562
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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