A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3442756



Internal ID14943023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89285684..89285886hg38UCSC Ensembl
Innerchr7:89285693..89285877hg38UCSC Ensembl
Outerchr7:89285675..89285895hg38UCSC Ensembl
chr7:88914998..88915200hg19UCSC Ensembl
Innerchr7:88915007..88915191hg19UCSC Ensembl
Outerchr7:88914989..88915209hg19UCSC Ensembl
chr7:88752934..88753136hg18UCSC Ensembl
Innerchr7:88752943..88753127hg18UCSC Ensembl
Outerchr7:88752925..88753145hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38203
hg19203
hg18203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8671468, essv8671467
SamplesNA19239, NA19240
Known GenesZNF804B
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3442756
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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