A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1600800



Internal ID12417235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26168427..26168427hg38UCSC Ensembl
chr7:26208047..26208047hg19UCSC Ensembl
chr7:26174572..26174572hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38120
hg19120
hg18120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3943401
SamplesHuRef
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1600800
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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