A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3903328



Internal ID11858543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19939786..19939885hg38UCSC Ensembl
chr6:19940017..19940116hg19UCSC Ensembl
chr6:20047996..20048095hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38100
hg19100
hg18100
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1337473
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3903328
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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