A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132197



Internal ID18926818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:179638165..179638965hg38UCSC Ensembl
Outerchr1:179607300..179608100hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv226n106
Supporting Variantsnssv3986926
SamplesKWS1
Known GenesTDRD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132197
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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