A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12891841



Internal ID2825274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93697862..93702887hg38UCSC Ensembl
Innerchr7:93697862..93702887hg38UCSC Ensembl
Outerchr7:93697362..93703387hg38UCSC Ensembl
chr7:93327174..93332199hg19UCSC Ensembl
Innerchr7:93327174..93332199hg19UCSC Ensembl
Outerchr7:93326674..93332699hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385026
hg195026
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614168
Supporting Variants
SamplesHG02493
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12891841
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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