A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706980



Internal ID21379256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237681669..237681940hg38UCSC Ensembl
chr2:238590312..238590583hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390250
Supporting Variants
Samples
Known GenesLRRFIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706980
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0229885


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