A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925634



Internal ID22700861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61218310..61218578hg38UCSC Ensembl
chr9:43602165..43602426hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38269
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925634
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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