A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997816



Internal ID18810666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909763..16931176hg38UCSC Ensembl
Innerchr1:17236258..17257671hg19UCSC Ensembl
Innerchr1:17108845..17130258hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821414
hg1921414
hg1821414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n100
Supporting Variantsnssv3464479
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)nsv997816
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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