A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257524



Internal ID20824564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26037420..26038177hg38UCSC Ensembl
chr2:26260289..26261046hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548427
Supporting Variants
Samples
Known GenesRAB10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257524
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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