A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516423



Internal ID15443716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156646228..156652883hg38UCSC Ensembl
Innerchr4:157567380..157574035hg19UCSC Ensembl
Innerchr4:157786830..157793485hg18UCSC Ensembl
Innerchr4:157924985..157931640hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386656
hg196656
hg186656
hg176656
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668279, nssv700143, nssv681131, nssv694102, nssv662970, nssv679880, nssv656863
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516423
Frequency
Sample Size2026
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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