A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969769



Internal ID18604996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29107490..29139956hg38UCSC Ensembl
Innerchr9:29107488..29139954hg19UCSC Ensembl
Innerchr9:29097488..29129954hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3832467
hg1932467
hg1832467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763416
SamplesHGDP00542
Known GenesLINGO2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969769
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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