A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3954954



Internal ID19207684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:78277504..78277560hg38UCSC Ensembl
Outerchr17:76273585..76273641hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109107
Supporting Variants
SamplesKWS1
Known GenesLOC100996291
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3954954
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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