A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005741



Internal ID71442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152113682..152113734hg38UCSC Ensembl
chr7:151810767..151810819hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142253
Supporting Variants
Samples
Known GenesGALNT11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005741
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006256


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