A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3588437



Internal ID12173430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58074277..58074454hg38UCSC Ensembl
chr17:56151638..56151815hg19UCSC Ensembl
chr17:53506637..53506814hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38178
hg19178
hg18178
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1398603
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3588437
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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