A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997286



Internal ID19156824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58739388..58767022hg38UCSC Ensembl
Innerchr4:59605553..59633187hg19UCSC Ensembl
Innerchr4:59300310..59327944hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3827635
hg1927635
hg1827635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739491
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997286
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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