A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677877



Internal ID15414529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:23651593..23711207hg38UCSC Ensembl
Innerchr4:23653216..23712830hg19UCSC Ensembl
Innerchr4:23262314..23321928hg18UCSC Ensembl
Innerchr4:23329485..23389099hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3859615
hg1959615
hg1859615
hg1759615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517733
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677877
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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