A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110808



Internal ID19282974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101417570..101417634hg38UCSC Ensembl
Outerchr7:101060851..101060915hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961217
SamplesKWS1
Known GenesCOL26A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110808
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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