A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434951



Internal ID22492821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90069895..90076277hg38UCSC Ensembl
chr8:91082123..91088505hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg386383
hg196383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925447
Supporting Variants
Samples
Known GenesCALB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434951
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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