A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976142



Internal ID22751077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155890514..155931331hg38UCSC Ensembl
chrX:155120177..155160995hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3840818
hg1940819
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435685
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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