A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3566982



Internal ID6691678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20624328..20624494hg38UCSC Ensembl
chr19:20807134..20807300hg19UCSC Ensembl
chr19:20598974..20599140hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38167
hg19167
hg18167
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010023
Supporting Variants
SamplesHuRef
Known GenesZNF626
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3566982
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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