A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4089908



Internal ID11325281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15337639..15337639hg38UCSC Ensembl
chr10:15379638..15379638hg19UCSC Ensembl
chr10:15419644..15419644hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1057266
Supporting Variants
SamplesHuRef
Known GenesFAM171A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4089908
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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