A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15623002



Internal ID3919972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14765272..15181525hg38UCSC Ensembl
chr17:14668589..15084842hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38416254
hg19416254
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640045
Supporting Variants
SamplesHG03572
Known GenesCDRT7, CDRT8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15623002
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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