A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336521



Internal ID20994074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5960595..5960749hg38UCSC Ensembl
chr2:6100727..6100881hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088769
Samples
Known GenesLINC01105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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