A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014417



Internal ID18756951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16912960..16931436hg38UCSC Ensembl
Innerchr1:17239455..17257931hg19UCSC Ensembl
Innerchr1:17112042..17130518hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3818477
hg1918477
hg1818477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv125n100
Supporting Variantsnssv3469094, nssv3476549, nssv3467829, nssv3471411
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)nsv1014417
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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