A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1495430



Internal ID12658552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113621714..113621796hg38UCSC Ensembl
chr6:113942916..113942998hg19UCSC Ensembl
chr6:114049609..114049691hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3883
hg1983
hg1883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3888671
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1495430
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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