A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527791



Internal ID15455084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176572527..176583124hg38UCSC Ensembl
Innerchr5:175999528..176010125hg19UCSC Ensembl
Innerchr5:175932134..175942731hg18UCSC Ensembl
Innerchr5:175932134..175942731hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3810598
hg1910598
hg1810598
hg1710598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704283
Samples
Known GenesCDHR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527791
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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