A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035618



Internal ID20602658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33422410..33423076hg38UCSC Ensembl
chr17:31749428..31750094hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507927
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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