A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1063912



Internal ID12227037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82975078..82975139hg38UCSC Ensembl
chr17:80932954..80933015hg19UCSC Ensembl
chr17:78526243..78526304hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3862
hg1962
hg1862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4271230
SamplesHuRef
Known GenesB3GNTL1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1063912
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer