A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903009



Internal ID22678173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136261761..136398939hg38UCSC Ensembl
chr2:137019331..137156509hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38137179
hg19137179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903009
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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