A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121836



Internal ID18937687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:61924924..61925268hg38UCSC Ensembl
Outerchr1:62390596..62390940hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv93n106
Supporting Variantsnssv3968488
SamplesKWS1
Known GenesINADL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121836
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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