A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138653



Internal ID20705693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120630701..120632300hg38UCSC Ensembl
chr6:120951847..120953446hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614286
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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