A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15626556



Internal ID5628372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15787620..15891380hg38UCSC Ensembl
chr17:15690934..15794694hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38103761
hg19103761
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640086
Supporting Variants
SamplesHG03166
Known GenesMEIS3P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15626556
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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