A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614931



Internal ID7001823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126334896..126534697hg38UCSC Ensembl
chr7:125974950..126174751hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38199802
hg19199802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12954069
SamplesNA18988
Known GenesGRM8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614931
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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