A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025541



Internal ID19114759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11966626..12007395hg38UCSC Ensembl
Innerchr5:11966738..12007507hg19UCSC Ensembl
Innerchr5:12019738..12060507hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3840770
hg1940770
hg1840770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638201
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)nsv1025541
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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