A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1065122



Internal ID12228247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67771161..67771217hg38UCSC Ensembl
chr15:68063499..68063555hg19UCSC Ensembl
chr15:65850553..65850609hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3803276
SamplesHuRef
Known GenesMAP2K5
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1065122
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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