A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967778



Internal ID18895551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:90397656..90398256hg38UCSC Ensembl
Outerchr14:90864000..90864600hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131072
Supporting Variants
SamplesKWS2
Known GenesCALM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967778
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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