A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035245



Internal ID20602285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37734288..37735679hg38UCSC Ensembl
chr17:36094277..36095669hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381392
hg191393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513070
Supporting Variants
Samples
Known GenesHNF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035245
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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