A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4159787



Internal ID11442325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118198240..118198240hg38UCSC Ensembl
chr10:119957752..119957752hg19UCSC Ensembl
chr10:119947742..119947742hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38104
hg19104
hg18104
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1573329
Supporting Variants
SamplesHuRef
Known GenesCASC2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4159787
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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