A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144307



Internal ID18933323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137618648..137619248hg38UCSC Ensembl
Outerchr9:140513100..140513700hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995045
SamplesKWS1
Known GenesC9orf37, EHMT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144307
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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