A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765396



Internal ID18962458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109680177..109702078hg38UCSC Ensembl
chr1:110222799..110244700hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3821902
hg1921902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077552
Supporting Variants
SamplesKWP1
Known GenesGSTM1, GSTM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765396
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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