A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982004



Internal ID19210627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39335903..39445500hg38UCSC Ensembl
Outerchr9:39335900..39462600hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38109598
hg19126701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119198
Supporting Variants
SamplesKWS1
Known GenesLOC653501, SPATA31A1, SPATA31A2, ZNF658B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982004
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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