A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526313



Internal ID15106920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:96667755..96994882hg38UCSC Ensembl
Innerchr2:97333492..97660619hg19UCSC Ensembl
Innerchr2:96697219..97024346hg18UCSC Ensembl
Innerchr2:96755366..97082493hg17UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38327128
hg19327128
hg18327128
hg17327128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702597
Samples
Known GenesANKRD23, ANKRD39, CNNM3, CNNM4, FAM178B, FER1L5, LMAN2L, MIR3127, SEMA4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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