A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109905



Internal ID19257680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101489605..101489701hg38UCSC Ensembl
Outerchr7:101132886..101132982hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958325
SamplesKWS1
Known GenesCOL26A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109905
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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