A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137635



Internal ID19259391
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 StatusM
Merged Variants
Supporting Variantsnssv3990136
SamplesKWS2
Known GenesFAM74A1, SPATA31A1, SPATA31A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137635
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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