A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119578



Internal ID19265688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:60935628..61003887hg38UCSC Ensembl
Outerchr9:41521900..41611000hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3868260
hg1989101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982009
SamplesKWS1
Known GenesLOC653501, ZNF658B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119578
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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