A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874088



Internal ID22649038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90927082..90927138hg38UCSC Ensembl
chr1:91392639..91392695hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405574
Samples
Known GenesZNF644
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874088
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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