A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1159587



Internal ID11976025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81734332..81735089hg38UCSC Ensembl
chr1:82200017..82200774hg19UCSC Ensembl
chr1:81972605..81973362hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38758
hg19758
hg18758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3870215
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1159587
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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