A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1502705



Internal ID12319141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:676241..676516hg38UCSC Ensembl
chr6:676241..676516hg19UCSC Ensembl
chr6:621241..621516hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38276
hg19276
hg18276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3999957
SamplesHuRef
Known GenesEXOC2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1502705
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