A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12889141



Internal ID2349879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91857444..91883636hg38UCSC Ensembl
Innerchr7:91857444..91883636hg38UCSC Ensembl
Outerchr7:91856944..91884136hg38UCSC Ensembl
chr7:91486758..91512950hg19UCSC Ensembl
Innerchr7:91486758..91512950hg19UCSC Ensembl
Outerchr7:91486258..91513450hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3826193
hg1926193
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614130
Supporting Variants
SamplesHG02084
Known GenesMTERF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12889141
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