A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5401127



Internal ID8966158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4898713..4900074hg38UCSC Ensembl
Outerchr7:4898676..4900124hg38UCSC Ensembl
Innerchr7:4938344..4939705hg19UCSC Ensembl
Outerchr7:4938307..4939755hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381449
hg191449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667895
Supporting Variants
SamplesHG00536
Known GenesMMD2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5401127
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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