A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990932



Internal ID20557972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40794646..40802415hg38UCSC Ensembl
chr11:40816196..40823965hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387770
hg197770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468129
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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