A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602690



Internal ID20975761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15714721..15722331hg38UCSC Ensembl
chr7:15754346..15761956hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg387611
hg197611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602690
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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