A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968097



Internal ID18892103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:179638153..179638924hg38UCSC Ensembl
Outerchr1:179607288..179608059hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113196
Supporting Variants
SamplesKWS2
Known GenesTDRD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968097
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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