A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137663



Internal ID18907098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92978318..92978918hg38UCSC Ensembl
Outerchr9:95740600..95741200hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982036, nssv3990165
SamplesKWS1, KWS2
Known GenesFGD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137663
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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