A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010398



Internal ID18752929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151789173..151818464hg38UCSC Ensembl
Innerchr1:151761649..151790940hg19UCSC Ensembl
Innerchr1:150028273..150057564hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3829292
hg1929292
hg1829292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3493239
Samples
Known GenesLINGO4, RORC, TDRKH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010398
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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