A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13522567



Internal ID3524387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74129821..74131974hg38UCSC Ensembl
Innerchr9:74129838..74131958hg38UCSC Ensembl
Outerchr9:74129805..74131991hg38UCSC Ensembl
chr9:76744737..76746890hg19UCSC Ensembl
Innerchr9:76744754..76746874hg19UCSC Ensembl
Outerchr9:76744721..76746907hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620692
Supporting Variants
SamplesHG02555
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13522567
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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