A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1637561



Internal ID12453995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91293455..91293455hg38UCSC Ensembl
chr14:91759799..91759799hg19UCSC Ensembl
chr14:90829552..90829552hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38168
hg19168
hg18168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4071862
SamplesHuRef
Known GenesCCDC88C
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1637561
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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