A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614256



Internal ID7001151
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12905063, essv12905062
SamplesHG03246, NA19072
Known GenesBAIAP2L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614256
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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