A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362751



Internal ID22588420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73722053..73722293hg38UCSC Ensembl
chr11:73433098..73433338hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907690
Supporting Variants
Samples
Known GenesRAB6A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362751
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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