A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937506



Internal ID22712875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77862757..77870073hg38UCSC Ensembl
chr17:75858839..75866155hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg387317
hg197317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937506
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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