A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126429



Internal ID18922227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:58463296..58463696hg38UCSC Ensembl
Outerchr16:58497200..58497600hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984677
SamplesKWS1
Known GenesNDRG4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126429
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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