A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770021



Internal ID19307847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150762512..150763913hg38UCSC Ensembl
chr3:150480299..150481700hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074633
Supporting Variants
SamplesKWP1
Known GenesSIAH2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770021
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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