A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968609



Internal ID18880957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76240319..76240619hg38UCSC Ensembl
Outerchr17:74236400..74236700hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121940
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968609
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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