A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967161



Internal ID19227072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:88256769..88257269hg38UCSC Ensembl
Outerchr15:88800000..88800500hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112675
Supporting Variants
SamplesKWS2
Known GenesNTRK3-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967161
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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