A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614255



Internal ID7001150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98364211..98364559hg38UCSC Ensembl
Innerchr7:98364213..98364557hg38UCSC Ensembl
Outerchr7:98364209..98364561hg38UCSC Ensembl
chr7:97993523..97993871hg19UCSC Ensembl
Innerchr7:97993525..97993869hg19UCSC Ensembl
Outerchr7:97993521..97993873hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12905061, essv12905059, essv12905060
SamplesHG01389, NA19681, NA19679
Known GenesBAIAP2L1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614255
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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