A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976829



Internal ID22751764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15499354..15500007hg38UCSC Ensembl
chr3:15540861..15541514hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424806
Samples
Known GenesCOLQ
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976829
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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