A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696718



Internal ID15433370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80872671..80897521hg38UCSC Ensembl
Innerchr4:81793825..81818675hg19UCSC Ensembl
Innerchr4:82012849..82037699hg18UCSC Ensembl
Innerchr4:82151004..82175854hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3824851
hg1924851
hg1824851
hg1724851
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517072
Supporting Variants
Samples
Known GenesC4orf22
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696718
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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