A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015657



Internal ID19104875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143747111..143870954hg38UCSC Ensembl
Innerchr7:143444204..143568047hg19UCSC Ensembl
Innerchr7:143075137..143198980hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38123844
hg19123844
hg18123844
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6717n100
Supporting Variantsnssv3670969, nssv3670967, nssv3670968, nssv3670957, nssv3670971, nssv3670976, nssv3670961, nssv3670970, nssv3670972, nssv3670956, nssv3670965, nssv3670974, nssv3754797, nssv3670975, nssv3670585, nssv3670586, nssv3754796, nssv3670963, nssv3670964, nssv3754795, nssv3670962, nssv3670959, nssv3670966, nssv3670958, nssv3670960, nssv3670973
Samples
Known GenesCTAGE6, FAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015657
Frequency
Sample Size11257
Observed Gain19
Observed Loss7
Observed Complex0
Frequencyn/a


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