A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498736



Internal ID20871949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41808695..41809550hg38UCSC Ensembl
chr17:39964947..39965802hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035514
Samples
Known GenesLEPREL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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