A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035203



Internal ID20602243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28806088..28811376hg38UCSC Ensembl
chr17:27133106..27138394hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385289
hg195289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501512
Supporting Variants
Samples
Known GenesFAM222B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035203
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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