A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521024



Internal ID15101631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74672139..74673233hg38UCSC Ensembl
Innerchr5:73967964..73969058hg19UCSC Ensembl
Innerchr5:74003720..74004814hg18UCSC Ensembl
Innerchr5:74003720..74004814hg17UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg381095
hg191095
hg181095
hg171095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680022, nssv682003, nssv692158
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521024
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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