A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767162



Internal ID19310832
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 StatusS
Merged Variantsnsv1073302
Supporting Variants
SamplesKWP1
Known GenesCOL26A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767162
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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