A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613833



Internal ID7000728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79317318..79329057hg38UCSC Ensembl
Innerchr7:79317353..79329022hg38UCSC Ensembl
Outerchr7:79317283..79329092hg38UCSC Ensembl
chr7:78946634..78958373hg19UCSC Ensembl
Innerchr7:78946669..78958338hg19UCSC Ensembl
Outerchr7:78946599..78958408hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3811740
hg1911740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12860384
SamplesHG01682
Known GenesMAGI2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613833
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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