A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985721



Internal ID18865543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:19855838..19855908hg38UCSC Ensembl
Outerchr13:20429978..20430048hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127310
Supporting Variants
SamplesKWS1
Known GenesZMYM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985721
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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