A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002017



Internal ID18744548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909177..16931176hg38UCSC Ensembl
Innerchr1:17235672..17257671hg19UCSC Ensembl
Innerchr1:17108259..17130258hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3822000
hg1922000
hg1822000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n100
Supporting Variantsnssv3470906, nssv3471741, nssv3469721, nssv3465805, nssv3480242, nssv3465241
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002017
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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