A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4241950



Internal ID11524488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1170779..1170779hg38UCSC Ensembl
chr5:1170894..1170894hg19UCSC Ensembl
chr5:1223894..1223894hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1419931
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4241950
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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