A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4330089



Internal ID11265941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1396818..1396900hg38UCSC Ensembl
chr10:1439013..1439095hg19UCSC Ensembl
chr10:1429013..1429095hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3883
hg1983
hg1883
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1082929
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4330089
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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