A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523341



Internal ID15103948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3720081..3723036hg38UCSC Ensembl
Innerchr18:3720081..3723036hg19UCSC Ensembl
Innerchr18:3710081..3713036hg18UCSC Ensembl
Innerchr18:3710081..3713036hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382956
hg192956
hg182956
hg172956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699088
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523341
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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