A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517503



Internal ID15444796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7630603..7638179hg38UCSC Ensembl
Innerchr4:7632330..7639906hg19UCSC Ensembl
Innerchr4:7683230..7690806hg18UCSC Ensembl
Innerchr4:7750401..7757977hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg387577
hg197577
hg187577
hg177577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656522, nssv652206
Samples
Known GenesSORCS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517503
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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