A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994087



Internal ID20561127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65052554..65056797hg38UCSC Ensembl
chr11:64820026..64824269hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg384244
hg194244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461701
Supporting Variants
Samples
Known GenesNAALADL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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