A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061324



Internal ID19150543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30407329..30442625hg38UCSC Ensembl
Innerchr18:27987295..28022591hg19UCSC Ensembl
Innerchr18:26241293..26276589hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3835297
hg1935297
hg1835297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564154
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)nsv1061324
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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