A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614638



Internal ID7001531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112930323..112977168hg38UCSC Ensembl
chr7:112570378..112617223hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3846846
hg1946846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12931122
SamplesNA19098
Known GenesC7orf60
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614638
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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