A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977915



Internal ID22752851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86525777..88855329hg38UCSC Ensembl
chr7:86155093..88484643hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382329553
hg192329551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447835
Samples
Known GenesABCB1, ABCB4, ADAM22, C7orf62, CROT, DBF4, DMTF1, GRM3, KIAA1324L, RUNDC3B, SLC25A40, SRI, STEAP4, TMEM243, TP53TG1, ZNF804B
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977915
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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