A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1678363



Internal ID12494795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9773959..9774030hg38UCSC Ensembl
chr16:9867816..9867887hg19UCSC Ensembl
chr16:9775317..9775388hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4011077
SamplesHuRef
Known GenesGRIN2A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1678363
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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