A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001678



Internal ID18744209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107117748..107155038hg38UCSC Ensembl
Innerchr1:107660370..107697660hg19UCSC Ensembl
Innerchr1:107461893..107499183hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3837291
hg1937291
hg1837291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3501027
Samples
Known GenesNTNG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001678
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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