A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967681



Internal ID18891322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:156081709..156082409hg38UCSC Ensembl
Outerchr1:156051500..156052200hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130977
Supporting Variants
SamplesKWS2
Known GenesMEX3A, MIR7851
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967681
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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