A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577102



Internal ID20950173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67279757..67280852hg38UCSC Ensembl
chr15:67572095..67573190hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381096
hg191096
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2572n223
Supporting Variantsnssv18238961
Samples
Known GenesIQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577102
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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