A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110831



Internal ID22020064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30631350..31029521hg38UCSC Ensembl
chr17:28958368..29356539hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38398172
hg19398172
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626126
Samples
Known GenesADAP2, ATAD5, CRLF3, DPRXP4, LRRC37BP1, RNF135, SUZ12P1, TEFM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110831
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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