A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4172629



Internal ID11108481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:676807..676862hg38UCSC Ensembl
chr6:676807..676862hg19UCSC Ensembl
chr6:621807..621862hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1105432
Supporting Variants
SamplesHuRef
Known GenesEXOC2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4172629
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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