A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341649



Internal ID20999202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71086677..71090866hg38UCSC Ensembl
chr2:71313807..71317996hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg384190
hg194190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341649
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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