A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3710604



Internal ID12051266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132404031..132404083hg38UCSC Ensembl
chr10:134217535..134217587hg19UCSC Ensembl
chr10:134067525..134067577hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1344000
Supporting Variants
SamplesHuRef
Known GenesPWWP2B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3710604
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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