A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497975



Internal ID20871183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33759178..33765329hg38UCSC Ensembl
chr17:32086197..32092348hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386152
hg196152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035026
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497975
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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