A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064626



Internal ID19153845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37925226..37961380hg38UCSC Ensembl
Innerchr18:35505190..35541344hg19UCSC Ensembl
Innerchr18:33759188..33795342hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3836155
hg1936155
hg1836155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564212
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064626
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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