A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764232



Internal ID19309167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16438584..16440122hg38UCSC Ensembl
chr1:16765079..16766617hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381539
hg191539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077130
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764232
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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