A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126982



Internal ID18937829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:24162726..24162778hg38UCSC Ensembl
Outerchr1:24489216..24489268hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv62n106
Supporting Variantsnssv3985272
SamplesKWS1
Known GenesIFNLR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126982
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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