A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544029



Internal ID20917270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75815812..75816693hg38UCSC Ensembl
chr1:76281497..76282378hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv244n223
Supporting Variantsnssv18253134
Samples
Known GenesMSH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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