A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049765



Internal ID101071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88520526..88524260hg38UCSC Ensembl
chr11:88253694..88257428hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383735
hg193735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512397
Supporting Variants
Samples
Known GenesGRM5, GRM5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049765
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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