A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977631



Internal ID19237808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63288428..63316328hg38UCSC Ensembl
Outerchr9:67243400..67271300hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3827901
hg1927901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115822
Supporting Variants
SamplesKWS2
Known GenesAQP7P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977631
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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