A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615115



Internal ID6655314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135148990..135156413hg38UCSC Ensembl
Innerchr7:135148990..135156413hg38UCSC Ensembl
Outerchr7:135148842..135156788hg38UCSC Ensembl
chr7:134833742..134841165hg19UCSC Ensembl
Innerchr7:134833742..134841165hg19UCSC Ensembl
Outerchr7:134833594..134841540hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg387424
hg197424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12975953
SamplesNA18633
Known GenesTMEM140
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615115
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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