A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3571395



Internal ID6696091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35196037..35196086hg38UCSC Ensembl
chr5:35196139..35196188hg19UCSC Ensembl
chr5:35231896..35231945hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008308
Supporting Variants
SamplesHuRef
Known GenesPRLR
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3571395
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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