A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527603



Internal ID15108210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40124074..40128134hg38UCSC Ensembl
Innerchr11:40145624..40149684hg19UCSC Ensembl
Innerchr11:40102200..40106260hg18UCSC Ensembl
Innerchr11:40102200..40106260hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384061
hg194061
hg184061
hg174061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704065
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527603
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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