A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115758



Internal ID18905347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100950066..100962777hg38UCSC Ensembl
Outerchr7:100547700..100554600hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3812712
hg196901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3626n106
Supporting Variantsnssv3977565
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115758
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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