A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614033



Internal ID20987104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123322465..123355630hg38UCSC Ensembl
chr7:122962519..122995684hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3833166
hg1933166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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