A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526955



Internal ID15454248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130921284..130965226hg38UCSC Ensembl
Innerchr4:131842439..131886381hg19UCSC Ensembl
Innerchr4:132061889..132105831hg18UCSC Ensembl
Innerchr4:132200044..132243986hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3843943
hg1943943
hg1843943
hg1743943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703327
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526955
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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