A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606860



Internal ID20979931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104005778..104024715hg38UCSC Ensembl
chr7:103646225..103665162hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3818938
hg1918938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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