A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1771073



Internal ID17737450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:65228446..65229878hg38UCSC Ensembl
Innerchr1:65694129..65695561hg19UCSC Ensembl
Innerchr1:65466717..65468149hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381433
hg191433
hg181433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv945984
Supporting Variants
SamplesHGDP00456
Known GenesAK4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1771073
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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