A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565078



Internal ID20938149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20636521..20637689hg38UCSC Ensembl
chr7:20676144..20677312hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381169
hg191169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273881
Samples
Known GenesABCB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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