A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607178



Internal ID6647420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151420015..151420720hg38UCSC Ensembl
Innerchr5:151420065..151420670hg38UCSC Ensembl
Outerchr5:151419905..151420830hg38UCSC Ensembl
chr5:150799576..150800281hg19UCSC Ensembl
Innerchr5:150799626..150800231hg19UCSC Ensembl
Outerchr5:150799466..150800391hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12099830
SamplesHG02050
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607178
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