A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701592



Internal ID15091558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57714251..57832787hg38UCSC Ensembl
Innerchr16:57748163..57866691hg19UCSC Ensembl
Innerchr16:56305664..56424192hg18UCSC Ensembl
Innerchr16:56305664..56424192hg17UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38118537
hg19118529
hg18118529
hg17118529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525464
Supporting Variants
Samples
Known GenesCCDC135, KATNB1, KIFC3, LOC388282, MIR6772
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701592
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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