A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521029



Internal ID15101636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112996530..112996626hg38UCSC Ensembl
Innerchr4:113917686..113917782hg19UCSC Ensembl
Innerchr4:114137135..114137231hg18UCSC Ensembl
Innerchr4:114275290..114275386hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3897
hg1997
hg1897
hg1797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697743
Samples
Known GenesANK2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521029
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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