A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3705563



Internal ID19003844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:245223553..245351437hg38UCSC Ensembl
Innerchr1:245386855..245514739hg19UCSC Ensembl
Innerchr1:243453478..243581362hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38127885
hg19127885
hg18127885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001831
Supporting Variants
Samples
Known GenesKIF26B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3705563
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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