A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15625083



Internal ID3004599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15648414..15672186hg38UCSC Ensembl
chr17:15551728..15575500hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3823773
hg1923773
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640078
Supporting Variants
SamplesHG02649
Known GenesTRIM16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15625083
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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