A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597645



Internal ID16385054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:26540207..28477865hg38UCSC Ensembl
Innerchr5:26540316..28477972hg19UCSC Ensembl
Innerchr5:26576073..28513729hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg381937659
hg191937657
hg181937657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153043
SamplesHGDP01255
Known GenesCDH9, LINC01021
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597645
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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