A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614253



Internal ID7001148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98323619..98325847hg38UCSC Ensembl
Innerchr7:98323619..98325847hg38UCSC Ensembl
Outerchr7:98323451..98326024hg38UCSC Ensembl
chr7:97952931..97955159hg19UCSC Ensembl
Innerchr7:97952931..97955159hg19UCSC Ensembl
Outerchr7:97952763..97955336hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382229
hg192229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12905057
SamplesNA12413
Known GenesBAIAP2L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614253
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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