A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662177



Internal ID15052143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76556311..77008124hg38UCSC Ensembl
Innerchr7:76185628..76637441hg19UCSC Ensembl
Innerchr7:76023564..76475377hg18UCSC Ensembl
Innerchr7:75830279..76282092hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38451814
hg19451814
hg18451814
hg17451814
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517634
Supporting Variants
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100133091, POMZP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662177
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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