A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535855



Internal ID20909209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173165419..173165935hg38UCSC Ensembl
chr2:174030147..174030663hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18256118
Samples
Known GenesZAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535855
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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