A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614397



Internal ID7001291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104579982..104609603hg38UCSC Ensembl
chr7:104220429..104250050hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3829622
hg1929622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1315e214
Supporting Variantsessv12913309, essv12913311, essv12913310, essv12913307, essv12913308
SamplesHG03986, NA19036, NA19445, HG03755, NA19429
Known GenesLHFPL3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614397
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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