A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4239180



Internal ID11175032
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1774334
Supporting Variants
SamplesHuRef
Known GenesNOP14
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4239180
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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