A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13549574



Internal ID3693341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88923548..88924120hg38UCSC Ensembl
Innerchr9:88923549..88924119hg38UCSC Ensembl
Outerchr9:88923547..88924121hg38UCSC Ensembl
chr9:91538463..91539035hg19UCSC Ensembl
Innerchr9:91538464..91539034hg19UCSC Ensembl
Outerchr9:91538462..91539036hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38573
hg19573
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621017
Supporting Variants
SamplesHG03297
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13549574
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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