A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6344595



Internal ID9321998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129445789..129446741hg38UCSC Ensembl
Outerchr7:129445752..129446791hg38UCSC Ensembl
Innerchr7:129085630..129086582hg19UCSC Ensembl
Outerchr7:129085593..129086632hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg381040
hg191040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674446
Supporting Variants
SamplesNA12154
Known GenesSTRIP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6344595
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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