A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602275



Internal ID20975346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51868995..51876830hg38UCSC Ensembl
chr7:51936691..51944526hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg387836
hg197836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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