A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767971



Internal ID19306830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30391796..30392197hg38UCSC Ensembl
chr15:30683999..30684400hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071199
Supporting Variants
SamplesKWP1
Known GenesCHRFAM7A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767971
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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