A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570531



Internal ID20943602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30204059..30204917hg38UCSC Ensembl
chr7:30243675..30244533hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6635n223
Supporting Variantsnssv18273462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570531
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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