A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849996



Internal ID22624931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74987413..74998124hg38UCSC Ensembl
chr8:75899648..75910359hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3810712
hg1910712
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509881
Samples
Known GenesCRISPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849996
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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