A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662363



Internal ID15052329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189310262..189407436hg38UCSC Ensembl
Innerchr4:190231416..190328590hg19UCSC Ensembl
Innerchr4:190468410..190565584hg18UCSC Ensembl
Innerchr4:190606565..190703739hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3897175
hg1997175
hg1897175
hg1797175
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517295
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662363
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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