A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6238338



Internal ID9215741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88493086..88493346hg38UCSC Ensembl
chr16:88559494..88559754hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671819
Supporting Variants
SamplesHG00699
Known GenesZFPM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6238338
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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