A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757351



Internal ID20533211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43322312..43385444hg38UCSC Ensembl
chr17:41399675..41462812hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3863133
hg1963138
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv45n199
Supporting Variantsnssv16268374
Samples
Known GenesLINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757351
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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