A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762386



Internal ID19315408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:726762..727963hg38UCSC Ensembl
chr7:766399..767600hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073622
Supporting Variants
SamplesKWP1
Known GenesHEATR2, PRKAR1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762386
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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