A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170306



Internal ID21314367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80627071..80635198hg38UCSC Ensembl
Outerchr10:80625285..80635559hg38UCSC Ensembl
Innerchr10:82386827..82394954hg19UCSC Ensembl
Outerchr10:82385041..82395315hg19UCSC Ensembl
Innerchr10:82376807..82384934hg18UCSC Ensembl
Outerchr10:82375021..82385295hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3810275
hg1910275
hg1810275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246445
SamplesSNI_9
Known GenesSH2D4B
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170306
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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