A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897170



Internal ID22672269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173932450..173936277hg38UCSC Ensembl
chr2:174797178..174801005hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383828
hg193828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393631
Samples
Known GenesSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897170
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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