A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1774334



Internal ID12590766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2960882..2960943hg38UCSC Ensembl
chr4:2962609..2962670hg19UCSC Ensembl
chr4:2932407..2932468hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3862
hg1962
hg1862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4239180
SamplesHuRef
Known GenesNOP14
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1774334
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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