A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071230



Internal ID19316047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84748368..84748869hg38UCSC Ensembl
chr15:85291599..85292100hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770037
SamplesKWP1
Known GenesZNF592
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071230
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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