A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075972



Internal ID19324619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74979558..75065788hg38UCSC Ensembl
chr7:74393699..74481600hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3886231
hg1987902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765729
SamplesKWP1
Known GenesWBSCR16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075972
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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