A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077124



Internal ID19317738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67644892..67656660hg38UCSC Ensembl
chr9:46303399..46315200hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811769
hg1911802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767359
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077124
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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