A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012484



Internal ID18755017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16561560..16637038hg38UCSC Ensembl
Innerchr1:16888055..16963533hg19UCSC Ensembl
Innerchr1:16760642..16836120hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3875479
hg1975479
hg1875479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv56n100
Supporting Variantsnssv3473239
Samples
Known GenesCROCCP2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012484
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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