A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925740



Internal ID22700967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70638984..70639405hg38UCSC Ensembl
chr8:71551219..71551640hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431066
Samples
Known GenesLACTB2, LOC286190
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925740
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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