A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18118209



Internal ID20685249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61013573..61019879hg38UCSC Ensembl
chr4:61879291..61885597hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg386307
hg196307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18118209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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