A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073302



Internal ID19318483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101415910..101417019hg38UCSC Ensembl
chr7:101059191..101060300hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767162
SamplesKWP1
Known GenesCOL26A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073302
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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