A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147408



Internal ID346589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75798237..75798885hg38UCSC Ensembl
chr17:73794318..73794966hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714661
Samples
Known GenesUNK
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147408
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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