A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034748



Internal ID20601788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3032951..3033315hg38UCSC Ensembl
chr17:2936245..2936609hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513454
Supporting Variants
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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