A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430466



Internal ID22488336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73440763..73441636hg38UCSC Ensembl
chr7:72855093..72855966hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970718
Supporting Variants
Samples
Known GenesBAZ1B
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430466
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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