A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507239



Internal ID20880527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2832384..2850468hg38UCSC Ensembl
chr17:2735678..2753762hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3818085
hg1918085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035185
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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