A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947084



Internal ID22722585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75297920..75304537hg38UCSC Ensembl
chr17:73294001..73300618hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg386618
hg196618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947084
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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