A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958684



Internal ID18864238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:141747538..141747596hg38UCSC Ensembl
Outerchr7:141447338..141447396hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128369
Supporting Variants
SamplesKWS1
Known GenesSSBP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958684
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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