A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968019



Internal ID18889836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:59640572..59641423hg38UCSC Ensembl
Outerchr1:60106244..60107095hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38852
hg19852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113124
Supporting Variants
SamplesKWS2
Known GenesFGGY
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968019
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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