A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619786



Internal ID7006660
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13408082, essv13408083, essv13408087, essv13408085, essv13408086, essv13408084, essv13408088
SamplesHG03449, NA20346, HG01779, HG01762, HG01148, NA19401, NA19116
Known GenesCCDC171
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619786
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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