A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736165



Internal ID20512111
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 StatusM
Merged Variants
Supporting Variantsnssv16286808
Samples
Known GenesIQCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736165
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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