A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615049



Internal ID16055772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103527145..104134528hg38UCSC Ensembl
Innerchr9:106289427..106896809hg19UCSC Ensembl
Innerchr9:105329248..105936630hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38607384
hg19607383
hg18607383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176103
Samples1780862339_A
Known GenesMIR6130, SMC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615049
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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