A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4172604



Internal ID11455142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13542148..13542308hg38UCSC Ensembl
chr6:13542380..13542540hg19UCSC Ensembl
chr6:13650359..13650519hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38161
hg19161
hg18161
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1262080
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4172604
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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