A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695069



Internal ID15431721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11072804..11172161hg38UCSC Ensembl
Innerchr4:11074428..11173785hg19UCSC Ensembl
Innerchr4:10683526..10782883hg18UCSC Ensembl
Innerchr4:10750697..10850054hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3899358
hg1999358
hg1899358
hg1799358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522287
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695069
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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