A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3468399



Internal ID19062815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10307274..10317913hg38UCSC Ensembl
Innerchr1:10367332..10377971hg19UCSC Ensembl
Innerchr1:10289919..10300558hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3810640
hg1910640
hg1810640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003027
Supporting Variants
Samples
Known GenesKIF1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3468399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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