A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035386



Internal ID20602426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30589766..30625383hg38UCSC Ensembl
chr17:28916784..28952401hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3835618
hg1935618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497748
Supporting Variants
Samples
Known GenesLRRC37BP1, SH3GL1P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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