A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1659194



Internal ID5789294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6277122..6277384hg38UCSC Ensembl
chr6:6277355..6277617hg19UCSC Ensembl
chr6:6222354..6222616hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38263
hg19263
hg18263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4313841
SamplesHuRef
Known GenesF13A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1659194
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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