A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349383



Internal ID21006936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:121157503..121167813hg38UCSC Ensembl
chr2:121915079..121925389hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3810311
hg1910311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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