A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562127



Internal ID335086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34097872..34108195hg38UCSC Ensembl
chr17:32424891..32435214hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810324
hg1910324
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712741
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562127
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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