A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968405



Internal ID18896437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:23929910..24036510hg38UCSC Ensembl
Outerchr1:24256400..24363000hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38106601
hg19106601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121756
Supporting Variants
SamplesKWS2
Known GenesPNRC2, SRSF10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968405
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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