A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13408087



Internal ID6001897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15595661..15600039hg38UCSC Ensembl
Innerchr9:15595661..15600039hg38UCSC Ensembl
Outerchr9:15595497..15600148hg38UCSC Ensembl
chr9:15595659..15600037hg19UCSC Ensembl
Innerchr9:15595659..15600037hg19UCSC Ensembl
Outerchr9:15595495..15600146hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg384379
hg194379
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619786
Supporting Variants
SamplesNA19401
Known GenesCCDC171
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13408087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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