A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969278



Internal ID18888469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:2621600..2622200hg38UCSC Ensembl
Outerchr9:2621600..2622200hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133705
Supporting Variants
SamplesKWS2
Known GenesFLJ35024, VLDLR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969278
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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