A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961217



Internal ID19209929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:101417570..101417634hg38UCSC Ensembl
Outerchr7:101060851..101060915hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110808
Supporting Variants
SamplesKWS1
Known GenesCOL26A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961217
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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