A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577802



Internal ID16018525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78979457..78980682hg38UCSC Ensembl
Innerchr18:76739457..76740682hg19UCSC Ensembl
Innerchr18:74840445..74841670hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381226
hg191226
hg181226
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6101n54
Supporting Variantsnssv888842
Samples
Known GenesSALL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577802
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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