A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273333



Internal ID20840373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25072527..28462755hg38UCSC Ensembl
chr7:25112146..28502373hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg383390229
hg193390228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562499
Supporting Variants
Samples
Known GenesC7orf31, C7orf71, CBX3, CREB5, CYCS, EVX1, HIBADH, HNRNPA2B1, HOTAIRM1, HOTTIP, HOXA1, HOXA10, HOXA10-HOXA9, HOXA11, HOXA11-AS, HOXA13, HOXA2, HOXA3, HOXA4, HOXA5, HOXA6, HOXA7, HOXA9, HOXA-AS3, HOXA-AS4, JAZF1, JAZF1-AS1, KIAA0087, LOC441204, MIR148A, MIR196B, NFE2L3, NPVF, RNU6-16P, SKAP2, SNX10, TAX1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273333
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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