A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140810



Internal ID19253643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:77992219..77992281hg38UCSC Ensembl
Outerchr7:77621536..77621598hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992316
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140810
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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