A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614062



Internal ID6654269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88957486..89061163hg38UCSC Ensembl
Innerchr7:88957510..89061139hg38UCSC Ensembl
Outerchr7:88957462..89061187hg38UCSC Ensembl
chr7:88586800..88690477hg19UCSC Ensembl
Innerchr7:88586824..88690453hg19UCSC Ensembl
Outerchr7:88586776..88690501hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38103678
hg19103678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12881167
SamplesNA19723
Known GenesZNF804B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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