A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542632



Internal ID20915890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25287799..25405616hg38UCSC Ensembl
chr1:25614290..25732107hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38117818
hg19117818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv131n223
Supporting Variantsnssv18251553
Samples
Known GenesRHCE, RHD, TMEM50A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542632
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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