A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010007



Internal ID18752538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169926141..169977295hg38UCSC Ensembl
Innerchr1:169895282..169946436hg19UCSC Ensembl
Innerchr1:168161906..168213060hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3851155
hg1951155
hg1851155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv461n100
Supporting Variantsnssv3489722
Samples
Known GenesKIFAP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010007
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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