A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968098



Internal ID18881593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:180656408..180656528hg38UCSC Ensembl
Outerchr1:180625544..180625664hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113197
Supporting Variants
SamplesKWS2
Known GenesXPR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968098
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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