A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15623554



Internal ID3919906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15027947..15074425hg38UCSC Ensembl
Innerchr17:15027947..15074425hg38UCSC Ensembl
Outerchr17:15027447..15074925hg38UCSC Ensembl
chr17:14931264..14977742hg19UCSC Ensembl
Innerchr17:14931264..14977742hg19UCSC Ensembl
Outerchr17:14930764..14978242hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3846479
hg1946479
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640051
Supporting Variants
SamplesHG03572
Known GenesCDRT7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15623554
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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