A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339411



Internal ID20996964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237774302..237783717hg38UCSC Ensembl
chr2:238682945..238692360hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg389416
hg199416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084406
Samples
Known GenesLRRFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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