A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617368



Internal ID20990439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13553731..13668363hg38UCSC Ensembl
chr7:13593356..13707988hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38114633
hg19114633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617368
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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