A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612556



Internal ID20985627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22832410..22862569hg38UCSC Ensembl
chr7:22872029..22902188hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3830160
hg1930160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154865
Samples
Known GenesSNORD93
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612556
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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