A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998363



Internal ID18811213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16876990..16965387hg38UCSC Ensembl
Innerchr1:17203485..17291882hg19UCSC Ensembl
Innerchr1:17076072..17164469hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3888398
hg1988398
hg1888398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv111n100
Supporting Variantsnssv3482416, nssv3470186
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)nsv998363
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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