A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517434



Internal ID20890795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56800101..56806200hg38UCSC Ensembl
chr17:54877462..54883561hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037023
Samples
Known GenesC17orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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