A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035957



Internal ID20602997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4705173..4705821hg38UCSC Ensembl
chr17:4608468..4609116hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505889
Supporting Variants
Samples
Known GenesLOC101559451
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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