A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077671



Internal ID18978272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:10755600..10755656hg38UCSC Ensembl
Outerchr17:10658917..10658973hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763565
SamplesKWP1
Known GenesTMEM220-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077671
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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