A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526855



Internal ID15454148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57785023..57786197hg38UCSC Ensembl
Innerchr16:57818935..57820109hg19UCSC Ensembl
Innerchr16:56376436..56377610hg18UCSC Ensembl
Innerchr16:56376436..56377610hg17UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381175
hg191175
hg181175
hg171175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703213
Samples
Known GenesKIFC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526855
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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