A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516731



Internal ID15097338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45172191..45185503hg38UCSC Ensembl
Innerchr7:45211790..45225102hg19UCSC Ensembl
Innerchr7:45178315..45191627hg18UCSC Ensembl
Innerchr7:44985030..44998342hg17UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3813313
hg1913313
hg1813313
hg1713313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv670497, nssv682815, nssv702001, nssv700467
Samples
Known GenesRAMP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516731
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer