A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764564



Internal ID19313223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149617616..149618418hg38UCSC Ensembl
chr1:149586799..149587600hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38803
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078936
Supporting Variants
SamplesKWP1
Known GenesLINC00623, LINC00869
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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