A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762232



Internal ID19307563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117202011..117202326hg38UCSC Ensembl
chr7:116842065..116842380hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076945
Supporting Variants
SamplesKWP1
Known GenesST7, ST7-OT3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762232
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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