A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978917



Internal ID22753852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61628784..61629478hg38UCSC Ensembl
chr2:61855919..61856613hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396405
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978917
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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