A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767059



Internal ID18961877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1610764..1611765hg38UCSC Ensembl
chr6:1610999..1612000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073531
Supporting Variants
SamplesKWP1
Known GenesFOXC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767059
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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