A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767294



Internal ID19309628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82321763..82344974hg38UCSC Ensembl
chr15:82614099..82640700hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3823212
hg1926602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069871
Supporting Variants
SamplesKWP1
Known GenesADAMTS7P1, GOLGA6L10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767294
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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