A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070830



Internal ID18974845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38673246..38673847hg38UCSC Ensembl
chr17:36829499..36830100hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771092
SamplesKWP1
Known GenesC17orf96
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070830
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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