A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704941



Internal ID15441593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107702503..107740646hg38UCSC Ensembl
Innerchr4:108623659..108661802hg19UCSC Ensembl
Innerchr4:108843108..108881251hg18UCSC Ensembl
Innerchr4:108981263..109019406hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3838144
hg1938144
hg1838144
hg1738144
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528356
Supporting Variants
Samples
Known GenesPAPSS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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