A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1098416



Internal ID12261540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:893850..893994hg38UCSC Ensembl
chr17:797090..797234hg19UCSC Ensembl
chr17:743840..743984hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38145
hg19145
hg18145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3696101
SamplesHuRef
Known GenesNXN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1098416
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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