A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562188



Internal ID20935259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66056081..66056571hg38UCSC Ensembl
chr7:65521068..65521558hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562188
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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