A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970231



Internal ID19245993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:155035694..155035758hg38UCSC Ensembl
Outerchr1:155008170..155008234hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133910
Supporting Variants
SamplesKWS2
Known GenesDCST1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970231
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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