A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957876



Internal ID18875169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:99550965..99551033hg38UCSC Ensembl
Outerchr7:99148588..99148656hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117743
Supporting Variants
SamplesKWS1
Known GenesFAM200A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957876
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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