A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12905063



Internal ID5660327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98388897..98390961hg38UCSC Ensembl
Innerchr7:98388921..98390937hg38UCSC Ensembl
Outerchr7:98388873..98390985hg38UCSC Ensembl
chr7:98018209..98020273hg19UCSC Ensembl
Innerchr7:98018233..98020249hg19UCSC Ensembl
Outerchr7:98018185..98020297hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382065
hg192065
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614256
Supporting Variants
SamplesNA19072
Known GenesBAIAP2L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12905063
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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