A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13556568



Internal ID1864580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91633520..91641005hg38UCSC Ensembl
Innerchr9:91633523..91641003hg38UCSC Ensembl
Outerchr9:91633518..91641008hg38UCSC Ensembl
chr9:94395802..94403287hg19UCSC Ensembl
Innerchr9:94395805..94403285hg19UCSC Ensembl
Outerchr9:94395800..94403290hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387486
hg197486
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621067
Supporting Variants
SamplesHG01765
Known GenesMIR3910-1, MIR3910-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13556568
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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