A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3870213



Internal ID11544972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1235477..1237977hg38UCSC Ensembl
chr10:1281413..1281581hg19UCSC Ensembl
chr10:1271413..1271581hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382501
hg19169
hg18169
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1541589
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3870213
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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