A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970969



Internal ID19214019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64086190..64086246hg38UCSC Ensembl
Outerchr15:64378389..64378445hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131193
Supporting Variants
SamplesKWS1
Known GenesFAM96A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970969
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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