A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256765



Internal ID20823805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127265088..127316221hg38UCSC Ensembl
chr2:128022664..128073797hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3851134
hg1951134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540759
Supporting Variants
Samples
Known GenesERCC3, MAP3K2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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