A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519932



Internal ID20893293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71832195..71837165hg38UCSC Ensembl
chr17:69828336..69833306hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg384971
hg194971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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