A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563231



Internal ID20936302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29613971..29615938hg38UCSC Ensembl
chr7:29653587..29655554hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381968
hg191968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6631n223
Supporting Variantsnssv18273445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563231
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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