A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517072



Internal ID15444365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80872671..80969196hg38UCSC Ensembl
Innerchr4:81793825..81890350hg19UCSC Ensembl
Innerchr4:82012849..82109374hg18UCSC Ensembl
Innerchr4:82151004..82247529hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3896526
hg1996526
hg1896526
hg1796526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653733, nssv671987, nssv687703, nssv691634, nssv684889, nssv670592, nssv654529, nssv673760, nssv679525, nssv690516, nssv658599, nssv668139, nssv662891, nssv654852, nssv670353, nssv687093, nssv667033, nssv696718, nssv664693, nssv665234, nssv681009, nssv651914, nssv681558, nssv661423, nssv656019, nssv657891, nssv656171, nssv690961, nssv693790, nssv674733, nssv673296, nssv684465, nssv675353, nssv656550, nssv660760
Samples
Known GenesC4orf22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517072
Frequency
Sample Size2026
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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