A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614278



Internal ID6654485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99482182..99483746hg38UCSC Ensembl
Innerchr7:99482236..99483693hg38UCSC Ensembl
Outerchr7:99482129..99483800hg38UCSC Ensembl
chr7:99079805..99081369hg19UCSC Ensembl
Innerchr7:99079859..99081316hg19UCSC Ensembl
Outerchr7:99079752..99081423hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12906308
SamplesNA18595
Known GenesZNF789
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614278
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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