A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957904



Internal ID18861822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:139379709..139379767hg38UCSC Ensembl
Outerchr7:139064455..139064513hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117762
Supporting Variants
SamplesKWS1
Known GenesC7orf55-LUC7L2, LUC7L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957904
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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