A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3705789



Internal ID18657384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46399305..46489856hg38UCSC Ensembl
Innerchr10:47035615..47150458hg19UCSC Ensembl
Innerchr10:46455621..46570464hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3890552
hg19114844
hg18114844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052733
Supporting Variants
Samples
Known GenesHNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3705789
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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