A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3689584



Internal ID12072286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75924555..75924607hg38UCSC Ensembl
chr6:76634272..76634324hg19UCSC Ensembl
chr6:76690992..76691044hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1561860
Supporting Variants
SamplesHuRef
Known GenesIMPG1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3689584
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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