A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4330730



Internal ID11613268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12355029..12355705hg38UCSC Ensembl
chr19:12465843..12466519hg19UCSC Ensembl
chr19:12326843..12327519hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38677
hg19677
hg18677
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1086965
Supporting Variants
SamplesHuRef
Known GenesZNF442
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4330730
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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