A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525664



Internal ID15452957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:108936420..108937139hg38UCSC Ensembl
Innerchr12:109330196..109330915hg19UCSC Ensembl
Innerchr12:107854325..107855044hg18UCSC Ensembl
Innerchr12:107832662..107833381hg17UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38720
hg19720
hg18720
hg17720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701820
Samples
Known GenesSVOP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525664
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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