A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061636



Internal ID19150855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44329344..44500755hg38UCSC Ensembl
Innerchr18:41909309..42080720hg19UCSC Ensembl
Innerchr18:40163307..40334718hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38171412
hg19171412
hg18171412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726069
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)nsv1061636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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