A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352056



Internal ID21009609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101303043..101307622hg38UCSC Ensembl
chr2:101919505..101924084hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg384580
hg194580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075490
Samples
Known GenesRNF149
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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