A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15625229



Internal ID5627045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15725032..15774926hg38UCSC Ensembl
Innerchr17:15725532..15774426hg38UCSC Ensembl
Outerchr17:15724032..15775926hg38UCSC Ensembl
chr17:15628346..15678240hg19UCSC Ensembl
Innerchr17:15628846..15677740hg19UCSC Ensembl
Outerchr17:15627346..15679240hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3849895
hg1949895
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640081
Supporting Variants
SamplesHG02406
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15625229
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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