A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615375



Internal ID16402784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127790636..127856098hg38UCSC Ensembl
Innerchr9:130552915..130618377hg19UCSC Ensembl
Innerchr9:129592736..129658198hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3865463
hg1965463
hg1865463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12880n54
Supporting Variantsnssv1176501
SamplesHGDP00688
Known GenesCDK9, ENG, FPGS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615375
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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