A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345361



Internal ID21002914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:179428461..179442409hg38UCSC Ensembl
chr2:180293188..180307136hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3813949
hg1913949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204688
Samples
Known GenesZNF385B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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