A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11639972



Internal ID1916585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144412455..144445713hg38UCSC Ensembl
chr4:145333607..145366865hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3833259
hg1933259
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602542
Supporting Variants
SamplesHG01795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11639972
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