A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498345



Internal ID20871555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44712687..44715445hg38UCSC Ensembl
chr17:42790055..42792813hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382759
hg192759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035863
Samples
Known GenesDBF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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