A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348391



Internal ID21005944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127460758..127471457hg38UCSC Ensembl
chr2:128218334..128229033hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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