A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3679025



Internal ID12082844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7207479..7207530hg38UCSC Ensembl
chr10:7249441..7249492hg19UCSC Ensembl
chr10:7289447..7289498hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1259186
Supporting Variants
SamplesHuRef
Known GenesSFMBT2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3679025
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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