A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990136



Internal ID19238289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:60864077..60956716hg38UCSC Ensembl
Outerchr9:39834300..39927200hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3892640
hg1992901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137635
Supporting Variants
SamplesKWS2
Known GenesFAM74A1, SPATA31A1, SPATA31A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990136
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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