A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109887



Internal ID18931364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:71296640..71296708hg38UCSC Ensembl
Outerchr7:70761626..70761694hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958295
SamplesKWS1
Known GenesWBSCR17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109887
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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