A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350193



Internal ID21007746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61671961..61675502hg38UCSC Ensembl
chr2:61899096..61902637hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg383542
hg193542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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