A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4160892



Internal ID11096744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:333274..333968hg38UCSC Ensembl
chr19:333274..333968hg19UCSC Ensembl
chr19:284274..284968hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38695
hg19695
hg18695
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1399571
Supporting Variants
SamplesHuRef
Known GenesMIER2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4160892
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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