A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3637447



Internal ID11777735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15775412..15775462hg38UCSC Ensembl
chr16:15869269..15869319hg19UCSC Ensembl
chr16:15776770..15776820hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1484275
Supporting Variants
SamplesHuRef
Known GenesMYH11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3637447
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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