A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539214



Internal ID20912518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28974785..28975903hg38UCSC Ensembl
chr1:29301297..29302415hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381119
hg191119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n223
Supporting Variantsnssv18252343
Samples
Known GenesEPB41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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