A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762216



Internal ID19313196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168136661..168136962hg38UCSC Ensembl
chr1:168105899..168106200hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1079039
Supporting Variants
SamplesKWP1
Known GenesGPR161
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762216
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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