A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520014



Internal ID18471609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31495114..31533123hg38UCSC Ensembl
Innerchr11:31516661..31554670hg19UCSC Ensembl
Innerchr11:31473237..31511246hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3838010
hg1938010
hg1838010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052451
Supporting Variants
Samples
Known GenesELP4, IMMP1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520014
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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