A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17396621



Internal ID22454491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4633902..4634318hg38UCSC Ensembl
chr2:4681492..4681908hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874318
Supporting Variants
Samples
Known GenesLOC727982
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17396621
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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