A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501237



Internal ID20874469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42596329..42601537hg38UCSC Ensembl
chr17:40748347..40753555hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg385209
hg195209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035641
Samples
Known GenesFAM134C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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