A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745831



Internal ID19044112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19017980..19282962hg38UCSC Ensembl
Innerchr5:19018089..19283071hg19UCSC Ensembl
Innerchr5:19053846..19318828hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38264983
hg19264983
hg18264983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032309
Supporting Variants
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)nssv3745831
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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