A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698862



Internal ID15435514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79026016..79027922hg38UCSC Ensembl
Innerchr4:79947170..79949076hg19UCSC Ensembl
Innerchr4:80166194..80168100hg18UCSC Ensembl
Innerchr4:80304349..80306255hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg381907
hg191907
hg181907
hg171907
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523154
Supporting Variants
Samples
Known GenesLINC01088
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698862
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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