A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137678



Internal ID19271204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136431148..136431948hg38UCSC Ensembl
Outerchr9:139325600..139326400hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4172n106
Supporting Variantsnssv3990179
SamplesKWS2
Known GenesINPP5E
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137678
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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