A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772996



Internal ID19308990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132925813..132950714hg38UCSC Ensembl
chr12:133502399..133527300hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3824902
hg1924902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070156
Supporting Variants
SamplesKWP1
Known GenesZNF605
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772996
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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