A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352835



Internal ID21010388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:137483850..137518617hg38UCSC Ensembl
chr2:138241420..138276187hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3834768
hg1934768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206599
Samples
Known GenesTHSD7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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