A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068703



Internal ID18975845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74607741..74614842hg38UCSC Ensembl
chr10:76367499..76374600hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg387102
hg197102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770872
SamplesKWP1
Known GenesADK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068703
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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