A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614894



Internal ID20987965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19870234..19870649hg38UCSC Ensembl
chr7:19909857..19910272hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614894
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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