A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923863



Internal ID22699090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43808438..43808493hg38UCSC Ensembl
chr7:43848037..43848092hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923863
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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