A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513402



Internal ID20886746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33474627..33475106hg38UCSC Ensembl
chr17:31801645..31802124hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035620
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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