A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1776644



Internal ID12593076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1641281..1641281hg38UCSC Ensembl
chr4:1643008..1643008hg19UCSC Ensembl
chr4:1612824..1612824hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38181
hg19181
hg18181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3605494
SamplesHuRef
Known GenesFAM53A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1776644
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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