A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346287



Internal ID21003840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173426216..173478954hg38UCSC Ensembl
chr2:174290944..174343682hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3852739
hg1952739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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