A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321169



Internal ID20854272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5691101..5694778hg38UCSC Ensembl
chr1:5751161..5754838hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg383678
hg193678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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