A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971081



Internal ID18878482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88501631..88501682hg38UCSC Ensembl
Outerchr16:88568039..88568090hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1131285
Supporting Variants
SamplesKWS1
Known GenesZFPM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971081
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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