A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769760



Internal ID19305636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14947792..14948793hg38UCSC Ensembl
chr3:14989299..14990300hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074573
Supporting Variants
SamplesKWP1
Known GenesFGD5-AS1, NR2C2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769760
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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