A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620480



Internal ID7007351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42905987..42912573hg38UCSC Ensembl
Innerchr9:42906017..42912542hg38UCSC Ensembl
Outerchr9:42905956..42912603hg38UCSC Ensembl
chr9:44058546..44065132hg19UCSC Ensembl
Innerchr9:44058577..44065102hg19UCSC Ensembl
Outerchr9:44058516..44065163hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386587
hg196587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13482415, essv13482414, essv13482418, essv13482417, essv13482416
SamplesNA12058, HG02703, HG03744, NA19707, HG03713
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620480
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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