A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034120



Internal ID20601160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18252585..18253588hg38UCSC Ensembl
chr17:18155899..18156902hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496915
Supporting Variants
Samples
Known GenesFLII
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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