A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562499



Internal ID20935570
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 StatusM
Merged Variants
Supporting Variantsnssv18273333
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)nsv6562499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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