A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598492



Internal ID6985628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165091032..165098406hg38UCSC Ensembl
Innerchr3:165091532..165097906hg38UCSC Ensembl
Outerchr3:165090032..165099406hg38UCSC Ensembl
chr3:164808820..164816194hg19UCSC Ensembl
Innerchr3:164809320..164815694hg19UCSC Ensembl
Outerchr3:164807820..164817194hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg387375
hg197375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11213440, essv11213438, essv11213442, essv11213444, essv11213441, essv11213436, essv11213437, essv11213439, essv11213443, essv11213445
SamplesHG02658, NA20853, HG04164, HG03873, HG03765, NA21124, HG03598, HG04186, HG03869, NA21090
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598492
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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