A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058632



Internal ID18801163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45721722..45758128hg38UCSC Ensembl
Innerchr20:44350361..44386767hg19UCSC Ensembl
Innerchr20:43783775..43820174hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3836407
hg1936407
hg1836400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4320n100
Supporting Variantsnssv3584931
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058632
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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