A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553697



Internal ID20926808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95047414..95047864hg38UCSC Ensembl
chr1:95512970..95513420hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253959
Samples
Known GenesALG14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553697
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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