A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1788130



Internal ID12604562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15979607..15979865hg38UCSC Ensembl
chr17:15882921..15883179hg19UCSC Ensembl
chr17:15823646..15823904hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38259
hg19259
hg18259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4080266
SamplesHuRef
Known GenesZSWIM7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1788130
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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