A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596700



Internal ID20969771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14912129..14973083hg38UCSC Ensembl
chr21:16284450..16345404hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3860955
hg1960955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254131
Samples
Known GenesNRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596700
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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