A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002401



Internal ID18744933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158742837..159002241hg38UCSC Ensembl
Innerchr1:158712627..158972031hg19UCSC Ensembl
Innerchr1:156979251..157238655hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38259405
hg19259405
hg18259405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3704744
Samples
Known GenesMNDA, OR6K6, OR6N1, OR6N2, PYHIN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002401
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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