A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3737311



Internal ID11677873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:501157..501418hg38UCSC Ensembl
chr6:501157..501418hg19UCSC Ensembl
chr6:446157..446418hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38262
hg19262
hg18262
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1476529
Supporting Variants
SamplesHuRef
Known GenesEXOC2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3737311
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