A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6122899



Internal ID9133222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148941624..148945330hg38UCSC Ensembl
Outerchr7:148941253..148945700hg38UCSC Ensembl
Innerchr7:148638716..148642422hg19UCSC Ensembl
Outerchr7:148638345..148642792hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384448
hg194448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671426
Supporting Variants
SamplesHG01173
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6122899
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer