A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390280



Internal ID22448150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87981038..88579778hg38UCSC Ensembl
chr1:88446721..89045461hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38598741
hg19598741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390280
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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