A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526300



Internal ID15106907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6980524..8391831hg38UCSC Ensembl
Innerchr18:6980523..8391829hg19UCSC Ensembl
Innerchr18:6970523..8381829hg18UCSC Ensembl
Innerchr18:6970523..8381829hg17UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg381411308
hg191411307
hg181411307
hg171411307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702581
Samples
Known GenesLAMA1, LOC100192426, LRRC30, PTPRM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526300
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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