A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611844



Internal ID6998746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2494048..2494741hg38UCSC Ensembl
Innerchr7:2494098..2494691hg38UCSC Ensembl
Outerchr7:2493998..2494791hg38UCSC Ensembl
chr7:2533682..2534375hg19UCSC Ensembl
Innerchr7:2533732..2534325hg19UCSC Ensembl
Outerchr7:2533632..2534425hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12668481
SamplesHG03472
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611844
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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