A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064279



Internal ID19153498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59878803..59925398hg38UCSC Ensembl
Innerchr20:58453858..58500453hg19UCSC Ensembl
Innerchr20:57887253..57933848hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3846596
hg1946596
hg1846596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4337n100
Supporting Variantsnssv3584303, nssv3584304
Samples
Known GenesSYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064279
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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