A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509881



Internal ID22567831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74987413..74998124hg38UCSC Ensembl
chr8:75899648..75910359hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3810712
hg1910712
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849996
Supporting Variants
Samples
Known GenesCRISPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509881
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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