A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126805



Internal ID19265428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101645820..101687020hg38UCSC Ensembl
Outerchr7:101289100..101330300hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3841201
hg1941201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3630n106
Supporting Variantsnssv3985078
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126805
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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