A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768586



Internal ID19308240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25957966..25958967hg38UCSC Ensembl
chr12:26110899..26111900hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069654
Supporting Variants
SamplesKWP1
Known GenesRASSF8-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768586
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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