A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739929



Internal ID20515904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101358746..101359080hg38UCSC Ensembl
chr2:101975208..101975542hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293789
Samples
Known GenesCREG2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739929
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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