A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4491061



Internal ID6735924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:5997691..6705136hg38UCSC Ensembl
Outerchr7:6037322..6744767hg19UCSC Ensembl
Outerchr7:6003848..6711292hg18UCSC Ensembl
Outerchr7:5810563..6518007hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38707446
hg19707446
hg18707445
hg17707445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1914954
Supporting Variants
Samples
Known GenesAIMP2, ANKRD61, C7orf26, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, PMS2, RAC1, USP42, ZDHHC4, ZNF12, ZNF316, ZNF853
MethodFISH
Analysis
PlatformFluorescent In-Situ Hybridization Instruments
Comments
ReferenceFeuk_et_al_2005
Pubmed ID16254605
Accession Number(s)essv4491061
Frequency
Sample Size18
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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