A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987788



Internal ID20554828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124146654..124147210hg38UCSC Ensembl
chr11:124017361..124017917hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455779
Supporting Variants
Samples
Known GenesVWA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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