A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121767



Internal ID19281342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109684378..109698778hg38UCSC Ensembl
Outerchr1:110227000..110241400hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3814401
hg1914401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv142n106
Supporting Variantsnssv3968416
SamplesKWS2
Known GenesGSTM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121767
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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