A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970492



Internal ID22745427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:63527575..63835888hg38UCSC Ensembl
chr7:62987953..63296266hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38308314
hg19308314
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447310
Samples
Known GenesMIR4283-1, MIR4283-2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970492
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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