A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3646964



Internal ID11768218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1368862..1368912hg38UCSC Ensembl
chr10:1411057..1411107hg19UCSC Ensembl
chr10:1401057..1401107hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1352224
Supporting Variants
SamplesHuRef
Known GenesADARB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3646964
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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