A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544991



Internal ID20918228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99343507..99343946hg38UCSC Ensembl
chr2:99959970..99960409hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258846
Samples
Known GenesEIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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