A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964381



Internal ID19234172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64371908..64372027hg38UCSC Ensembl
Outerchr15:64664107..64664226hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121155
Supporting Variants
SamplesKWS2
Known GenesKIAA0101
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964381
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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