A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998222



Internal ID18811072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16949734hg38UCSC Ensembl
Innerchr1:17203485..17276229hg19UCSC Ensembl
Innerchr1:17076072..17148816hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3872745
hg1972745
hg1872745
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv116n100
Supporting Variantsnssv3467375, nssv3466064, nssv3476966, nssv3700256, nssv3700254, nssv3463996, nssv3473138, nssv3700253, nssv3478822, nssv3700252, nssv3466125, nssv3467148, nssv3481465, nssv3478580, nssv3476579, nssv3700251, nssv3481664, nssv3481828, nssv3469230, nssv3700255, nssv3471151, nssv3467615, nssv3469351, nssv3472627, nssv3480934, nssv3473782
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)nsv998222
Frequency
Sample Size29084
Observed Gain23
Observed Loss3
Observed Complex0
Frequencyn/a


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