A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3927131



Internal ID11834741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32346006..32346329hg38UCSC Ensembl
chr6:32313783..32314106hg19UCSC Ensembl
chr6:32421761..32422084hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38324
hg19324
hg18324
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1081136
Supporting Variants
SamplesHuRef
Known GenesC6orf10
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3927131
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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