A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014777



Internal ID19103994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:244308789..244368778hg38UCSC Ensembl
Innerchr1:244472091..244532080hg19UCSC Ensembl
Innerchr1:242538714..242598703hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3859990
hg1959990
hg1859990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3498085
Samples
Known GenesC1orf100
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014777
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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