A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559760



Internal ID20932831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40044761..40046842hg38UCSC Ensembl
chr7:40084360..40086441hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6657n223
Supporting Variantsnssv18275272
Samples
Known GenesCDK13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559760
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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