A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12886885



Internal ID5611079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90796687..90798310hg38UCSC Ensembl
Innerchr7:90796689..90798308hg38UCSC Ensembl
Outerchr7:90796685..90798312hg38UCSC Ensembl
chr7:90426002..90427625hg19UCSC Ensembl
Innerchr7:90426004..90427623hg19UCSC Ensembl
Outerchr7:90426000..90427627hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614110
Supporting Variants
SamplesNA19041
Known GenesCDK14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12886885
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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