A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772302



Internal ID19314371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1637871..1637946hg38UCSC Ensembl
chr2:1641643..1641718hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072377
Supporting Variants
SamplesKWP1
Known GenesPXDN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772302
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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