A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765030



Internal ID18960824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23930209..24036410hg38UCSC Ensembl
chr1:24256699..24362900hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38106202
hg19106202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075339
Supporting Variants
SamplesKWP1
Known GenesPNRC2, SRSF10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765030
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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