A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612963



Internal ID6999862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42493710..42499419hg38UCSC Ensembl
Innerchr7:42493860..42499269hg38UCSC Ensembl
Outerchr7:42493560..42499569hg38UCSC Ensembl
chr7:42533309..42539018hg19UCSC Ensembl
Innerchr7:42533459..42538868hg19UCSC Ensembl
Outerchr7:42533159..42539168hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385710
hg195710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12752617
SamplesHG01710
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612963
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