A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612890



Internal ID6999789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38701514..38726622hg38UCSC Ensembl
chr7:38741114..38766222hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3825109
hg1925109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12744609
SamplesHG03598
Known GenesVPS41
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612890
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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