A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137631



Internal ID18926844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39184603..39364303hg38UCSC Ensembl
Outerchr9:39184600..39364300hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38179701
hg19179701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990132
SamplesKWS2
Known GenesCNTNAP3, SPATA31A1, SPATA31A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137631
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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