A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998355



Internal ID18811205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16470226..16643949hg38UCSC Ensembl
Innerchr1:16796721..16970444hg19UCSC Ensembl
Innerchr1:16669308..16843031hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38173724
hg19173724
hg18173724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv40n100
Supporting Variantsnssv3478940
Samples
Known GenesCROCCP2, CROCCP3, MIR3675, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998355
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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