A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595007



Internal ID16035730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:104948391..105445052hg38UCSC Ensembl
Innerchr4:105869548..106366209hg19UCSC Ensembl
Innerchr4:106088997..106585658hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38496662
hg19496662
hg18496662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153158
SamplesHGDP01035
Known GenesPPA2, TET2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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