A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614540



Internal ID7001433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110823772..110936663hg38UCSC Ensembl
Innerchr7:110823772..110936663hg38UCSC Ensembl
Outerchr7:110823272..110937163hg38UCSC Ensembl
chr7:110463828..110576719hg19UCSC Ensembl
Innerchr7:110463828..110576719hg19UCSC Ensembl
Outerchr7:110463328..110577219hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38112892
hg19112892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12926488
SamplesNA19391
Known GenesIMMP2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614540
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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