A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286808



Internal ID20496026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236356155..236356775hg38UCSC Ensembl
chr2:237264798..237265418hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736165
Supporting Variants
Samples
Known GenesIQCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286808
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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