A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771092



Internal ID18968150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38673246..38673847hg38UCSC Ensembl
chr17:36829499..36830100hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070830
Supporting Variants
SamplesKWP1
Known GenesC17orf96
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771092
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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