A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570365



Internal ID20943436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73254964..73255481hg38UCSC Ensembl
chr6:73964687..73965204hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274062
Samples
Known GenesKHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570365
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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