A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614215



Internal ID7001110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96509769..96511949hg38UCSC Ensembl
Innerchr7:96509782..96511937hg38UCSC Ensembl
Outerchr7:96509757..96511962hg38UCSC Ensembl
chr7:96139081..96141261hg19UCSC Ensembl
Innerchr7:96139094..96141249hg19UCSC Ensembl
Outerchr7:96139069..96141274hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382181
hg192181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12901196
SamplesNA19740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614215
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