A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539774



Internal ID20913069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77658165..77658512hg38UCSC Ensembl
chr1:78123850..78124197hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253157
Samples
Known GenesZZZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539774
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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