A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562605



Internal ID20935676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128202569..128206735hg38UCSC Ensembl
chr7:127842622..127846788hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg384167
hg194167
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562605
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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