A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347897



Internal ID21005450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:136467726..136472394hg38UCSC Ensembl
chr2:137225296..137229964hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg384669
hg194669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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