A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15624268



Internal ID5626084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15209141..15256214hg38UCSC Ensembl
chr17:15112458..15159531hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3847074
hg1947074
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640064
Supporting Variants
SamplesHG03572
Known GenesMIR4731, PMP22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15624268
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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