A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985191



Internal ID18856791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:91423618..91424018hg38UCSC Ensembl
Outerchr9:94185900..94186300hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126913
Supporting Variants
SamplesKWS1
Known GenesNFIL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985191
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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