A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12889037



Internal ID5970866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91703858..91704765hg38UCSC Ensembl
Innerchr7:91703951..91704661hg38UCSC Ensembl
Outerchr7:91703808..91704815hg38UCSC Ensembl
chr7:91333173..91334080hg19UCSC Ensembl
Innerchr7:91333266..91333976hg19UCSC Ensembl
Outerchr7:91333123..91334130hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614127
Supporting Variants
SamplesNA19380
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12889037
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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