A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557884



Internal ID20930955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97000063..97001388hg38UCSC Ensembl
chr7:96629375..96630700hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275759
Samples
Known GenesDLX6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557884
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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