A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1062832



Internal ID12225957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37037042..37037177hg38UCSC Ensembl
chr4:37038664..37038799hg19UCSC Ensembl
chr4:36715059..36715194hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38136
hg19136
hg18136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4272189
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1062832
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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