A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12903618



Internal ID6100043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97516458..97518219hg38UCSC Ensembl
Innerchr7:97516458..97518219hg38UCSC Ensembl
Outerchr7:97516344..97518337hg38UCSC Ensembl
chr7:97145770..97147531hg19UCSC Ensembl
Innerchr7:97145770..97147531hg19UCSC Ensembl
Outerchr7:97145656..97147649hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381762
hg191762
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614237
Supporting Variants
SamplesNA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12903618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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