A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498786



Internal ID20871999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6717101..6719200hg38UCSC Ensembl
chr17:6620420..6622519hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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