A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072702



Internal ID18975160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77247648..77249349hg38UCSC Ensembl
chr3:77296799..77298500hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771403
SamplesKWP1
Known GenesROBO2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072702
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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