A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060521



Internal ID18803052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36837185..36863491hg38UCSC Ensembl
Innerchr18:34417148..34443454hg19UCSC Ensembl
Innerchr18:32671146..32697452hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3826307
hg1926307
hg1826307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564203
Samples
Known GenesKIAA1328
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060521
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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