A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967030



Internal ID19244127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82958829..82958989hg38UCSC Ensembl
Outerchr17:80916705..80916865hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130712
Supporting Variants
SamplesKWS2
Known GenesB3GNTL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967030
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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