A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772430



Internal ID19308151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77697364..77698565hg38UCSC Ensembl
chr13:78271499..78272700hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070597
Supporting Variants
SamplesKWP1
Known GenesMIR3665, SLAIN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772430
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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