A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975312



Internal ID19232274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:132447767..132447827hg38UCSC Ensembl
Outerchr7:132132526..132132586hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115009
Supporting Variants
SamplesKWS2
Known GenesPLXNA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975312
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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