A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347648



Internal ID21005201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159095042..159202016hg38UCSC Ensembl
chr2:159951554..160058527hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38106975
hg19106974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205604
Samples
Known GenesMIR6888, TANC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347648
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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