A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110487



Internal ID18929018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:71602915..71604415hg38UCSC Ensembl
Outerchr7:71067900..71069400hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381501
hg191501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3586n106
Supporting Variantsnssv3960138
SamplesKWS1
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110487
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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