A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998713



Internal ID18811563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:35956942..36008597hg38UCSC Ensembl
Innerchr1:36422543..36474198hg19UCSC Ensembl
Innerchr1:36195130..36246785hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3851656
hg1951656
hg1851656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3479335
Samples
Known GenesAGO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998713
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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