A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4340494



Internal ID11276346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:675968..676076hg38UCSC Ensembl
chr6:675968..676076hg19UCSC Ensembl
chr6:620968..621076hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38109
hg19109
hg18109
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1416044
Supporting Variants
SamplesHuRef
Known GenesEXOC2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4340494
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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