A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6061679



Internal ID9341912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111046520..111071918hg38UCSC Ensembl
chr7:110686576..110711974hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3825399
hg1925399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673039
Supporting Variants
SamplesNA18539
Known GenesIMMP2L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6061679
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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