A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507572



Internal ID20880866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6384067..6394184hg38UCSC Ensembl
chr17:6287387..6297504hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3810118
hg1910118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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