A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140826



Internal ID18917914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100949827..100949899hg38UCSC Ensembl
Outerchr7:100547459..100547533hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3873
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975556, nssv3986744
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140826
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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