A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535137



Internal ID20908498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78622334..78622602hg38UCSC Ensembl
chr17:76618416..76618684hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038117
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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