A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369039



Internal ID22594708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46887649..46888139hg38UCSC Ensembl
chr11:46909200..46909690hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918103
Supporting Variants
Samples
Known GenesLRP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369039
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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