A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564590



Internal ID20937661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7997650..7998526hg38UCSC Ensembl
chr7:8037281..8038157hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276683
Samples
Known GenesGLCCI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564590
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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