A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509032



Internal ID20882337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43923797..43929031hg38UCSC Ensembl
chr17:42001165..42006399hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg385235
hg195235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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