A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909744



Internal ID22684954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77642488..77648080hg38UCSC Ensembl
chr7:77271805..77277397hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg385593
hg195593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909744
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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