A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038042



Internal ID19127261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31600987..31653728hg38UCSC Ensembl
Innerchr11:31622534..31675276hg19UCSC Ensembl
Innerchr11:31579110..31631852hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3852742
hg1952743
hg1852743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1090n100
Supporting Variantsnssv3504546
Samples
Known GenesELP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038042
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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