A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770025



Internal ID18958385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67709978..67710216hg38UCSC Ensembl
chr1:68175661..68175899hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077905
Supporting Variants
SamplesKWP1
Known GenesGNG12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770025
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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