A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1227822



Internal ID12044259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88000285..88001083hg38UCSC Ensembl
chr16:88033891..88034689hg19UCSC Ensembl
chr16:86591392..86592190hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4104629
SamplesHuRef
Known GenesBANP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1227822
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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