A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13003995



Internal ID5937538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149691217..149693757hg38UCSC Ensembl
Innerchr7:149691243..149693731hg38UCSC Ensembl
Outerchr7:149691191..149693783hg38UCSC Ensembl
chr7:149388308..149390848hg19UCSC Ensembl
Innerchr7:149388334..149390822hg19UCSC Ensembl
Outerchr7:149388282..149390874hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382541
hg192541
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615435
Supporting Variants
SamplesNA19350
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13003995
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