A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970459



Internal ID22745394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156601626..156608863hg38UCSC Ensembl
chr7:156394320..156401557hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg387238
hg197238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439116
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970459
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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