A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4242319



Internal ID11178171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1558615..1558615hg38UCSC Ensembl
chr10:1600810..1600810hg19UCSC Ensembl
chr10:1590810..1590810hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38177
hg19177
hg18177
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1437533
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4242319
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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