A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555970



Internal ID20929041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139600972..139601964hg38UCSC Ensembl
chr7:139285718..139286710hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38993
hg19993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274426
Samples
Known GenesHIPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555970
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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