A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614892



Internal ID7001785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125150198..125152516hg38UCSC Ensembl
Innerchr7:125150207..125152507hg38UCSC Ensembl
Outerchr7:125150189..125152525hg38UCSC Ensembl
chr7:124790252..124792570hg19UCSC Ensembl
Innerchr7:124790261..124792561hg19UCSC Ensembl
Outerchr7:124790243..124792579hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg382319
hg192319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12951382, essv12951383
SamplesHG03750, HG03697
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614892
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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