A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034376



Internal ID20601416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1428801..1430500hg38UCSC Ensembl
chr17:1332095..1333794hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498986
Supporting Variants
Samples
Known GenesCRK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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