A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614835



Internal ID7001728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122126760..122136302hg38UCSC Ensembl
Innerchr7:122126760..122136302hg38UCSC Ensembl
Outerchr7:122126399..122136667hg38UCSC Ensembl
chr7:121766814..121776356hg19UCSC Ensembl
Innerchr7:121766814..121776356hg19UCSC Ensembl
Outerchr7:121766453..121776721hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg389543
hg199543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12948437
SamplesHG00236
Known GenesAASS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614835
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer