A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733577



Internal ID20509507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237681676..237681948hg38UCSC Ensembl
chr2:238590319..238590591hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291762
Samples
Known GenesLRRFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733577
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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