A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987439



Internal ID19215408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:99586677..99598277hg38UCSC Ensembl
Outerchr7:99184300..99195900hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3811601
hg1911601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132652
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987439
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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