A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517765



Internal ID15098372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4311534..4313044hg38UCSC Ensembl
Innerchr18:4311534..4313044hg19UCSC Ensembl
Innerchr18:4301534..4303044hg18UCSC Ensembl
Innerchr18:4301534..4303044hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381511
hg191511
hg181511
hg171511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677260, nssv660670, nssv670910, nssv684672, nssv653156
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517765
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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