A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965722



Internal ID19243497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:81546418..81550514hg38UCSC Ensembl
Outerchr3:81595569..81599665hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg384097
hg194097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112040
Supporting Variants
SamplesKWS2
Known GenesGBE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965722
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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