A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148056



Internal ID20715096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88708260..88749288hg38UCSC Ensembl
chr6:89417979..89459007hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3841029
hg1941029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415535
Supporting Variants
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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