A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027775



Internal ID19116993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56714602..56886690hg38UCSC Ensembl
Innerchr7:56782295..56954387hg19UCSC Ensembl
Innerchr7:56749789..56921881hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38172089
hg19172093
hg18172093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6364n100
Supporting Variantsnssv3661429
Samples
Known GenesLOC100130849
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027775
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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