A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614214



Internal ID16401623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36901497..36922927hg38UCSC Ensembl
Innerchr9:36901494..36922924hg19UCSC Ensembl
Innerchr9:36891494..36912924hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3821431
hg1921431
hg1821431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176449
SamplesNINDS_173
Known GenesPAX5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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