A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341421



Internal ID20998974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27306702..27310488hg38UCSC Ensembl
chr2:27529570..27533356hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383787
hg193787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085697
Samples
Known GenesMPV17, TRIM54, UCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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