A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998178



Internal ID18811028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:145642988..145793384hg38UCSC Ensembl
Innerchr1:145641696..145792052hg19UCSC Ensembl
Innerchr1:144353053..144503409hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38150397
hg19150357
hg18150357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3498745
Samples
Known GenesCD160, GPR89A, LOC100288142, NBPF10, PDZK1, RNF115
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998178
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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