A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6505792



Internal ID9483195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155802622..155815928hg38UCSC Ensembl
Outerchr7:155802251..155816298hg38UCSC Ensembl
Innerchr7:155595316..155608622hg19UCSC Ensembl
Outerchr7:155594945..155608992hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3814048
hg1914048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663062
Supporting Variants
SamplesHG00421
Known GenesSHH
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6505792
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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