A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984447



Internal ID19223378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:143874049..143939629hg38UCSC Ensembl
Outerchr1:149368600..149434200hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3865581
hg1965601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126216
Supporting Variants
SamplesKWS1
Known GenesFCGR1C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984447
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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