A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024291



Internal ID19113508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:56070736..56111841hg38UCSC Ensembl
Innerchr5:55366563..55407668hg19UCSC Ensembl
Innerchr5:55402320..55443425hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3841106
hg1941106
hg1841106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642138
Samples
Known GenesANKRD55
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024291
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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