A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705348



Internal ID15442000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:154051916..154102791hg38UCSC Ensembl
Innerchr4:154973068..155023943hg19UCSC Ensembl
Innerchr4:155192518..155243393hg18UCSC Ensembl
Innerchr4:155330673..155381548hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3850876
hg1950876
hg1850876
hg1750876
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528701
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705348
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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