A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563648



Internal ID20936719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56375197..56375461hg38UCSC Ensembl
chr8:57287756..57288020hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278311
Samples
Known GenesSDR16C6P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563648
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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