A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737735



Internal ID20513698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118986599..118986662hg38UCSC Ensembl
chr2:119744175..119744238hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262115
Samples
Known GenesMARCO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737735
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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