A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975266



Internal ID18880876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:66203684..66203743hg38UCSC Ensembl
Outerchr7:65668671..65668730hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124220
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975266
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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