A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121786



Internal ID18916192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:180658964..180659664hg38UCSC Ensembl
Outerchr1:180628100..180628800hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv229n106
Supporting Variantsnssv3968436
SamplesKWS2
Known GenesXPR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121786
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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