A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070414



Internal ID18976032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65560381..65560882hg38UCSC Ensembl
chr17:63556499..63557000hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772027
SamplesKWP1
Known GenesAXIN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070414
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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