A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114978



Internal ID18926387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:74310915..74311014hg38UCSC Ensembl
Outerchr7:73725245..73725344hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975276
SamplesKWS2
Known GenesCLIP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114978
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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