A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502465



Internal ID20875710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42760901..42763300hg38UCSC Ensembl
chr17:40912919..40915318hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035652
Samples
Known GenesRAMP2, RAMP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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