A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003945



Internal ID18746476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16921166..16935740hg38UCSC Ensembl
Innerchr1:17247661..17262235hg19UCSC Ensembl
Innerchr1:17120248..17134822hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3814575
hg1914575
hg1814575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv126n100
Supporting Variantsnssv3467125
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)nsv1003945
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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