A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1632857



Internal ID12449291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7994082..7995181hg38UCSC Ensembl
chr4:7995809..7996908hg19UCSC Ensembl
chr4:8046709..8047808hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381100
hg191100
hg181100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4172806
SamplesHuRef
Known GenesABLIM2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1632857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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