A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500174



Internal ID20873399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36722101..36722600hg38UCSC Ensembl
chr17:35078412..35078911hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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