A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985211



Internal ID19209195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137439848..137441448hg38UCSC Ensembl
Outerchr9:140334300..140335900hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126932
Supporting Variants
SamplesKWS1
Known GenesENTPD8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985211
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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