A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762805



Internal ID18962619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180658963..180659764hg38UCSC Ensembl
chr1:180628099..180628900hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069123
Supporting Variants
SamplesKWP1
Known GenesXPR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762805
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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