A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562727



Internal ID20935798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134300321..134300918hg38UCSC Ensembl
chr6:134621459..134622056hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n223
Supporting Variantsnssv18271931
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562727
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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