A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3958649



Internal ID18860717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:80872567..80872630hg38UCSC Ensembl
Outerchr7:80501883..80501946hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128346
Supporting Variants
SamplesKWS1
Known GenesSEMA3C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3958649
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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