A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615635



Internal ID7002524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155727597..155733322hg38UCSC Ensembl
Innerchr7:155727597..155733322hg38UCSC Ensembl
Outerchr7:155727097..155733822hg38UCSC Ensembl
chr7:155520291..155526016hg19UCSC Ensembl
Innerchr7:155520291..155526016hg19UCSC Ensembl
Outerchr7:155519791..155526516hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385726
hg195726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13037693
SamplesHG02278
Known GenesRBM33
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615635
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